Stuart Schwartz

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Mefford Heather C; Sharp Andrew J; Baker Carl; Itsara Andy; Jiang Zhaoshi; Buysse Karen; Huang Shuwen; Maloney Viv K; Crolla John A; Baralle Diana; Collins Amanda; Mercer Catherine; Norga Koen; de Ravel Thomy; Devriendt Koen; Bongers Ernie M H F; de Leeuw Nicole; Reardon William; Gimelli Stefania; Bena Frederique; Hennekam Raoul C; Male Alison; Gaunt Lorraine; Clayton-Smith Jill; Simonic Ingrid; Park Soo Mi; Mehta Sarju G; Nik-Zainal Serena; Woods C Geoffrey; Firth Helen V; Parkin Georgina; Fichera Marco; Reitano Santina; Lo Giudice Mariangela; Li Kelly E; Casuga Iris; Broomer Adam; Conrad Bernard; Schwerzmann Markus; Räber Lorenz; Gallati Sabina; Striano Pasquale; Coppola Antonietta; Tolmie John L; Tobias Edward S; Lilley Chris; Armengol Lluis; Spysschaert Yves; Verloo Patrick; De Coene Anja; Goossens Linde; Mortier Geert; Speleman Frank; van Binsbergen Ellen; Nelen Marcel R; Hochstenbach Ron; Poot Martin; Gallagher Louise; Gill Michael; McClellan Jon; King Mary-Claire; Regan Regina; Skinner Cindy; Stevenson Roger E; Antonarakis Stylianos E; Chen Caifu; Estivill Xavier; Menten Björn; Gimelli Giorgio; Gribble Susan; Schwartz Stuart; Sutcliffe James S; Walsh Tom; Knight Samantha J L; Sebat Jonathan; Romano Corrado; Schwartz Charles E; Veltman Joris A; de Vries Bert B A; Vermeesch Joris R; Barber John C K; Willatt Lionel; Tassabehji May; Eichler Evan E
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
Nowaczyk Malgorzata J M; Carter Melissa T; Xu Jie; Huggins Marlene; Raca Gordana; Das Soma; Martin Christa Lese; Schwartz Stuart; Rosenfield Robert; Waggoner Darrel J
Paternal deletion 6q24.3: a new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearance.
Jagadeeswaran Ramasamy; Surawska Hanna; Krishnaswamy Soundararajan; Janamanchi Varalakshmi; Mackinnon A Craig; Seiwert Tanguy Y; Loganathan Sivakumar; Kanteti Rajani; Reichman Trevor; Nallasura Vidya; Schwartz Stuart; Faoro Leonardo; Wang Yi-Ching; Girard Luc; Tretiakova Maria S; Ahmed Salman; Zumba Osvaldo; Soulii Lioubov; Bindokas Vytas P; Szeto Livia L; Gordon Gavin J; Bueno Raphael; Sugarbaker David; Lingen Mark W; Sattler Martin; Krausz Thomas; Vigneswaran Wickii; Natarajan Viswanathan; Minna John; Vokes Everett E; Ferguson Mark K; Husain Aliya N; Salgia Ravi
Paxillin is a target for somatic mutations in lung cancer: implications for cell growth and invasion.

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2008: Mefford Heather C; Sharp Andrew J; Baker Carl; Itsara Andy; Jiang Zhaoshi; Buysse Karen; Huang Shuwen; Maloney Viv K; Crolla John A; Baralle Diana; Collins Amanda; Mercer Catherine; Norga Koen; de Ravel Thomy; Devriendt Koen; Bongers Ernie M H F; de Leeuw Nicole; Reardon William; Gimelli Stefania; Bena Frederique; Hennekam Raoul C; Male Alison; Gaunt Lorraine; Clayton-Smith Jill; Simonic Ingrid; Park Soo Mi; Mehta Sarju G; Nik-Zainal Serena; Woods C Geoffrey; Firth Helen V; Parkin Georgina; Fichera Marco; Reitano Santina; Lo Giudice Mariangela; Li Kelly E; Casuga Iris; Broomer Adam; Conrad Bernard; Schwerzmann Markus; Räber Lorenz; Gallati Sabina; Striano Pasquale; Coppola Antonietta; Tolmie John L; Tobias Edward S; Lilley Chris; Armengol Lluis; Spysschaert Yves; Verloo Patrick; De Coene Anja; Goossens Linde; Mortier Geert; Speleman Frank; van Binsbergen Ellen; Nelen Marcel R; Hochstenbach Ron; Poot Martin; Gallagher Louise; Gill Michael; McClellan Jon; King Mary-Claire; Regan Regina; Skinner Cindy; Stevenson Roger E; Antonarakis Stylianos E; Chen Caifu; Estivill Xavier; Menten Björn; Gimelli Giorgio; Gribble Susan; Schwartz Stuart; Sutcliffe James S; Walsh Tom; Knight Samantha J L; Sebat Jonathan; Romano Corrado; Schwartz Charles E; Veltman Joris A; de Vries Bert B A; Vermeesch Joris R; Barber John C K; Willatt Lionel; Tassabehji May; Eichler Evan E
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
The New England journal of medicine 2008;359(16):1685-99.
2008: Nowaczyk Malgorzata J M; Carter Melissa T; Xu Jie; Huggins Marlene; Raca Gordana; Das Soma; Martin Christa Lese; Schwartz Stuart; Rosenfield Robert; Waggoner Darrel J
Paternal deletion 6q24.3: a new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearance.
American journal of medical genetics. Part A 2008;146(3):354-60.
2008: Jagadeeswaran Ramasamy; Surawska Hanna; Krishnaswamy Soundararajan; Janamanchi Varalakshmi; Mackinnon A Craig; Seiwert Tanguy Y; Loganathan Sivakumar; Kanteti Rajani; Reichman Trevor; Nallasura Vidya; Schwartz Stuart; Faoro Leonardo; Wang Yi-Ching; Girard Luc; Tretiakova Maria S; Ahmed Salman; Zumba Osvaldo; Soulii Lioubov; Bindokas Vytas P; Szeto Livia L; Gordon Gavin J; Bueno Raphael; Sugarbaker David; Lingen Mark W; Sattler Martin; Krausz Thomas; Vigneswaran Wickii; Natarajan Viswanathan; Minna John; Vokes Everett E; Ferguson Mark K; Husain Aliya N; Salgia Ravi
Paxillin is a target for somatic mutations in lung cancer: implications for cell growth and invasion.
Cancer research 2008;68(1):132-42.
2007: Sharp Andrew J; Itsara Andy; Cheng Ze; Alkan Can; Schwartz Stuart; Eichler Evan E
Optimal design of oligonucleotide microarrays for measurement of DNA copy-number.
Human molecular genetics 2007;16(22):2770-9.
2007: Dempsey Melissa A; Schwartz Stuart; Waggoner Darrel J
Mosaicism del(22)(q11.2q11.2)/dup(22)(q11.2q11.2) in a patient with features of 22q11.2 deletion syndrome.
American journal of medical genetics. Part A 2007;143A(10):1082-6.
2006: Topping Daniel; Brown Petrice; Judis LuAnn; Schwartz Stuart; Seftel Allen; Thomas Anthony; Hassold Terry
Synaptic defects at meiosis I and non-obstructive azoospermia.
Human reproduction (Oxford, England) 2006;21(12):3171-7.
2006: Sharp Andrew J; Hansen Sierra; Selzer Rebecca R; Cheng Ze; Regan Regina; Hurst Jane A; Stewart Helen; Price Sue M; Blair Edward; Hennekam Raoul C; Fitzpatrick Carrie A; Segraves Rick; Richmond Todd A; Guiver Cheryl; Albertson Donna G; Pinkel Daniel; Eis Peggy S; Schwartz Stuart; Knight Samantha J L; Eichler Evan E
Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome.
Nature genetics 2006;38(9):1038-42.
2006: Graf M D; Christ L; Mascarello J T; Mowrey P; Pettenati M; Stetten G; Storto P; Surti U; Van Dyke D L; Vance G H; Wolff D; Schwartz S
Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study.
Journal of medical genetics 2006;43(8):660-4.
2006: Locke Devin P; Sharp Andrew J; McCarroll Steven A; McGrath Sean D; Newman Tera L; Cheng Ze; Schwartz Stuart; Albertson Donna G; Pinkel Daniel; Altshuler David M; Eichler Evan E
Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome.
American journal of human genetics 2006;79(2):275-90.
2006: Kulikowski Leslie D; Christ Laurie A; Nogueira Sintia I; Brunoni Decio; Schwartz Stuart; Melaragno Maria I
Breakpoint mapping in a case of mosaicism with partial monosomy 9p23 --> pter and partial trisomy 1q41 --> qter suggests neo-telomere formation in stabilizing the deleted chromosome.
American journal of medical genetics. Part A 2006;140(1):82-7.
2005: Brown Petrice W; Judis Luann; Chan E Ricky; Schwartz Stuart; Seftel Allen; Thomas Anthony; Hassold Terry J
Meiotic synapsis proceeds from a limited number of subtelomeric sites in the human male.
American journal of human genetics 2005;77(4):556-66.
2005: Mehra S; Christ L; Jeng L; Zinn A B; Schwartz S
Characterization of a familial balanced rec(13) in a child with mild MR and his half-sibling with two structurally rearranged chromosomes 13.
American journal of medical genetics. Part A 2005;137(2):217-21.
2005: Horvath Julie E; Gulden Cassandra L; Vallente Rhea U; Eichler Marla Y; Ventura Mario; McPherson John D; Graves Tina A; Wilson Richard K; Schwartz Stuart; Rocchi Mariano; Eichler Evan E
Punctuated duplication seeding events during the evolution of human chromosome 2p11.
Genome research 2005;15(7):914-27.
2005: Sharp Andrew J; Locke Devin P; McGrath Sean D; Cheng Ze; Bailey Jeffrey A; Vallente Rhea U; Pertz Lisa M; Clark Royden A; Schwartz Stuart; Segraves Rick; Oseroff Vanessa V; Albertson Donna G; Pinkel Daniel; Eichler Evan E
Segmental duplications and copy-number variation in the human genome.
American journal of human genetics 2005;77(1):78-88.
2005: Caudill Samuel P; Van Dyke Daniel L; Chen Andrew T L; Reidy John A; Ing Paul S; Schwartz Stuart; Vance Gail H
Evaluating current policy for detecting mosaicism in amniotic fluid cultures: implications for current cell counting practices.
Statistics in medicine 2005;24(4):615-22.
2005: Falk Marni J; Curtis Christine A; Bass Nancy E; Zinn Arthur B; Schwartz Stuart
Maternal uniparental disomy chromosome 14: case report and literature review.
Pediatric neurology 2005;32(2):116-20.
2004: She Xinwei; Horvath Julie E; Jiang Zhaoshi; Liu Ge; Furey Terrence S; Christ Laurie; Clark Royden; Graves Tina; Gulden Cassy L; Alkan Can; Bailey Jeff A; Sahinalp Cenk; Rocchi Mariano; Haussler David; Wilson Richard K; Miller Webb; Schwartz Stuart; Eichler Evan E
The structure and evolution of centromeric transition regions within the human genome.
Nature 2004;430(7002):857-64.
2004: Manning Melanie A; Cassidy Suzanne B; Clericuzio Carol; Cherry Athena M; Schwartz Stuart; Hudgins Louanne; Enns Gregory M; Hoyme H Eugene
Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrum.
Pediatrics 2004;114(2):451-7.
2004: Timur A Anil; Sadgephour Azita; Graf Michael; Schwartz Stuart; Libby Eric D; Driscoll David J; Wang Qing
Identification and molecular characterization of a de novo supernumerary ring chromosome 18 in a patient with Klippel-Trenaunay syndrome.
Annals of human genetics 2004;68(Pt 4):353-61.
2004: Chu Cathy; Schwartz Stuart; McPherson Elizabeth
Paternal uniparental isodisomy for chromosome 14 in a patient with a normal 46,XY karyotype.
American journal of medical genetics. Part A 2004;127A(2):167-71.
2004: Astbury Caroline; Christ Laurie A; Aughton David J; Cassidy Suzanne B; Fujimoto Atsuko; Pletcher Beth A; Schafer Irwin A; Schwartz Stuart
Delineation of complex chromosomal rearrangements: evidence for increased complexity.
Human genetics 2004;114(5):448-57.
2004: Astbury Caroline; Christ Laurie A; Aughton David J; Cassidy Suzanne B; Kumar Arun; Eichler Evan E; Schwartz Stuart
Detection of deletions in de novo "balanced" chromosome rearrangements: further evidence for their role in phenotypic abnormalities.
Genetics in medicine : official journal of the American College of Medical Genetics 2004;6(2):81-9.
2004: Locke D P; Segraves R; Nicholls R D; Schwartz S; Pinkel D; Albertson D G; Eichler E E
BAC microarray analysis of 15q11-q13 rearrangements and the impact of segmental duplications.
Journal of medical genetics 2004;41(3):175-82.
2004: Judis LuAnn; Chan Ernest R; Schwartz Stuart; Seftel Allen; Hassold Terry
Meiosis I arrest and azoospermia in an infertile male explained by failure of formation of a component of the synaptonemal complex.
Fertility and sterility 2004;81(1):205-9.
2004: Hassold T; Judis L; Chan E R; Schwartz S; Seftel A; Lynn A
Cytological studies of meiotic recombination in human males.
Cytogenetic and genome research 2004;107(3-4):249-55.
2003: Rudd M Katharine; Mays Robert W; Schwartz Stuart; Willard Huntington F
Human artificial chromosomes with alpha satellite-based de novo centromeres show increased frequency of nondisjunction and anaphase lag.
Molecular and cellular biology 2003;23(21):7689-97.
2003: Schwartz Stuart
Fishing for a better language.
Genetics in medicine : official journal of the American College of Medical Genetics 2003;5(5):345-6.
2003: Wolf Nancy G; Farver Carol; Abdul-Karim Fadi W; Schwartz Stuart
Analysis of microsatellite instability and X-inactivation in ovarian borderline tumors lacking numerical abnormalities by comparative genomic hybridization.
Cancer genetics and cytogenetics 2003;145(2):133-8.
2003: Horvath J E; Gulden C L; Bailey J A; Yohn C; McPherson J D; Prescott A; Roe B A; de Jong P J; Ventura M; Misceo D; Archidiacono N; Zhao S; Schwartz S; Rocchi M; Eichler E E
Using a pericentromeric interspersed repeat to recapitulate the phylogeny and expansion of human centromeric segmental duplications.
Molecular biology and evolution 2003;20(9):1463-79.
2002: Graf Michael D; Gill Prabhcharan; Krew Michael; Schwartz Stuart
Prenatal detection of structural abnormalities of chromosome 18: associations with interphase fluorescence in situ hybridization (FISH) and maternal serum screening.
Prenatal diagnosis 2002;22(8):645-8.
2002: Bailey Jeffrey A; Gu Zhiping; Clark Royden A; Reinert Knut; Samonte Rhea V; Schwartz Stuart; Adams Mark D; Myers Eugene W; Li Peter W; Eichler Evan E
Recent segmental duplications in the human genome.
Science (New York, N.Y.) 2002;297(5583):1003-7.
2002: Lynn Audrey; Koehler Kara E; Judis LuAnn; Chan Ernest R; Cherry Jonathan P; Schwartz Stuart; Seftel Allen; Hunt Patricia A; Hassold Terry J
Covariation of synaptonemal complex length and mammalian meiotic exchange rates.
Science (New York, N.Y.) 2002;296(5576):2222-5.
2002: Liu Lili; Schwartz Stuart; Davis Brian M; Gerson Stanton L
Chemotherapy-induced O(6)-benzylguanine-resistant alkyltransferase mutations in mismatch-deficient colon cancer.
Cancer research 2002;62(11):3070-6.
2002: Pettenati Mark J; Von Kap-Herr Chris; Jackle Bethy; Bobby Peggy; Mowrey Philip; Schwartz Stuart; Rao P Nagesh; Rosnes Jon
Rapid interphase analysis for prenatal diagnosis of translocation carriers using subtelomeric probes.
Prenatal diagnosis 2002;22(3):193-7.
2002: Li Hui; Myeroff Lois; Kasturi Lakshmi; Krumroy Lisa; Schwartz Stuart; Willson James K V; Stanbridge Eric; Casey Graham; Markowitz Sanford
Chromosomal autonomy of hMLH1 methylation in colon cancer.
Oncogene 2002;21(9):1443-9.
2002: Satinover David L; Schwartz Stuart
Clinical application of PRINS.
American journal of medical genetics 2002;107(2):95-6.
2002: Bailey Jeffrey A; Yavor Amy M; Viggiano Luigi; Misceo Doriana; Horvath Juliann E; Archidiacono Nicoletta; Schwartz Stuart; Rocchi Mariano; Eichler Evan E
Human-specific duplication and mosaic transcripts: the recent paralogous structure of chromosome 22.
American journal of human genetics 2002;70(1):83-100.
2002: Colmenares Clemencia; Heilstedt Heidi A; Shaffer Lisa G; Schwartz Stuart; Berk Michael; Murray Jeffrey C; Stavnezer Ed
Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski-/- mice.
Nature genetics 2002;30(1):106-9.
2002: Schwartz Stuart; Graf Michael D
Microdeletion syndromes. Characteristics and diagnosis.
Methods in molecular biology (Clifton, N.J.) 2002;204():275-90.
2002: Graf Michael D; Schwartz Stuart
Molecular approaches for delineating marker chromosomes.
Methods in molecular biology (Clifton, N.J.) 2002;204():211-8.
2001: Gunay-Aygun M; Schwartz S; Heeger S; O'Riordan M A; Cassidy S B
The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria.
Pediatrics 2001;108(5):E92.
2001: Schafer I A; Robin N H; Posch J J; Clark B A; Izumo S; Schwartz S
Distal 5q deletion syndrome: phenotypic correlations.
American journal of medical genetics 2001;103(1):63-8.
2001: Satinover D L; Vance G H; Van Dyke D L; Schwartz S
Cytogenetic analysis and construction of a BAC contig across a common neocentromeric region from 9p.
Chromosoma 2001;110(4):275-83.
2001: Alagramam K N; Yuan H; Kuehn M H; Murcia C L; Wayne S; Srisailpathy C R; Lowry R B; Knaus R; Van Laer L; Bernier F P; Schwartz S; Lee C; Morton C C; Mullins R F; Ramesh A; Van Camp G; Hageman G S; Woychik R P; Smith R J;
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F.
Human molecular genetics 2001;10(16):1709-18.
2001: Hassold T J; Burrage L C; Chan E R; Judis L M; Schwartz S; James S J; Jacobs P A; Thomas N S
Maternal folate polymorphisms and the etiology of human nondisjunction.
American journal of human genetics 2001;69(2):434-9.
2001: Riley D; Wiznitzer M; Schwartz S; Zinn A B
A 13-year-old boy with cognitive impairment, retinoblastoma, and Wilson disease.
Neurology 2001;57(1):141-3.
2001: Schwartz S; Micale M A; Becker L
Preparation of amniocytes for interphase fluorescence in situ hybridization (FISH).
Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.] 2001;Chapter 8():Unit 8.9.
2000: Wandstrat A E; Schwartz S
Isolation and molecular analysis of inv dup(15) and construction of a physical map of a common breakpoint in order to elucidate their mechanism of formation.
Chromosoma 2000;109(7):498-505.
2000: Chadwick L H; McCandless S E; Silverman G L; Schwartz S; Westaway D; Nadeau J H
Betaine-homocysteine methyltransferase-2: cDNA cloning, gene sequence, physical mapping, and expression of the human and mouse genes.
Genomics 2000;70(1):66-73.
2000: McCandless S E; Schwartz S; Morrison S; Garlapati K; Robin N H
Adult with an interstitial deletion of chromosome 10 [del(10)(q25. 1q25.3)]: overlap with Coffin-Lowry syndrome.
American journal of medical genetics 2000;95(2):93-8.
2000: Wandstrat A E; Conroy J M; Zurcher V L; Pasztor L M; Clark B A; Zackowski J L; Schwartz S
Molecular and cytogenetic analysis of familial Xp deletions.
American journal of medical genetics 2000;94(2):163-9.
2000: Teshima I; Bawle E V; Weksberg R; Shuman C; Van Dyke D L; Schwartz S
Analphoid 3qter markers.
American journal of medical genetics 2000;94(2):113-9.
2000: Pretlow T G; Schwartz S; Giaconia J M; Wright A L; Grimm H A; Edgehouse N L; Murphy J R; Markowitz S D; Jamison J M; Summers J L; Hamlin C R; MacLennan G T; Resnick M I; Pretlow T P; Connell C F
Prostate cancer and other xenografts from cells in peripheral blood of patients.
Cancer research 2000;60(15):4033-6.
2000: Horvath J E; Schwartz S; Eichler E E
The mosaic structure of human pericentromeric DNA: a strategy for characterizing complex regions of the human genome.
Genome research 2000;10(6):839-52.
2000: Warburton P E; Dolled M; Mahmood R; Alonso A; Li S; Naritomi K; Tohma T; Nagai T; Hasegawa T; Ohashi H; Govaerts L C; Eussen B H; Van Hemel J O; Lozzio C; Schwartz S; Dowhanick-Morrissette J J; Spinner N B; Rivera H; Crolla J A; Yu C; Warburton D
Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere.
American journal of human genetics 2000;66(6):1794-806.
2000: Ji Y; Eichler E E; Schwartz S; Nicholls R D
Structure of chromosomal duplicons and their role in mediating human genomic disorders.
Genome research 2000;10(5):597-610.
2000: Reddy K S; Sulcova V; Schwartz S; Noble J E; Phillips J; Brasel J A; Huff K; Lin H J
Mosaic tetrasomy 8q: inverted duplication of 8q23.3qter in an analphoid marker.
American journal of medical genetics 2000;92(1):69-76.
2000: Wolff D J; Schwartz S; Carrel L
Molecular determination of X inactivation pattern correlates with phenotype in women with a structurally abnormal X chromosome.
Genetics in medicine : official journal of the American College of Medical Genetics 2000;2(2):136-41.
2000: Dewald G; Stallard R; Alsaadi A; Arnold S; Blough R; Ceperich T M; Rafael Elejalde B; Fink J; Higgins J V; Higgins R R; Hoeltge G A; Hsu W T; Johnson E B; Kronberger D; McCorquodale D J; Meisner L F; Micale M A; Oseth L; Payne J S; Schwartz S; Sheldon S; Sophian A; Storto P; Van Tuinen P; Wenger G D; Wiktor A; Willis L A; Yung J F; Zenger-Hain J
A multicenter investigation with D-FISH BCR/ABL1 probes.
Cancer genetics and cytogenetics 2000;116(2):97-104.
1999: Marcelino J; Carpten J D; Suwairi W M; Gutierrez O M; Schwartz S; Robbins C; Sood R; Makalowska I; Baxevanis A; Johnstone B; Laxer R M; Zemel L; Kim C A; Herd J K; Ihle J; Williams C; Johnson M; Raman V; Alonso L G; Brunoni D; Gerstein A; Papadopoulos N; Bahabri S A; Trent J M; Warman M L
CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome.
Nature genetics 1999;23(3):319-22.
1999: Christ L A; Crowe C A; Micale M A; Conroy J M; Schwartz S
Chromosome breakage hotspots and delineation of the critical region for the 9p-deletion syndrome.
American journal of human genetics 1999;65(5):1387-95.
1999: Sirko-Osadsa D A; Cassidy S B; Depinet T W; Robin N H; Limwongse C; Schwartz S
Molecular refinement of karyotype: beyond the cytogenetic band.
Genetics in medicine : official journal of the American College of Medical Genetics 1999;1(6):254-61.
1999: Saller D N; Canick J A; Blitzer M G; Palomaki G E; Schwartz S; Blakemore K J; Haddow J E
Second-trimester maternal serum analyte levels associated with fetal trisomy 13.
Prenatal diagnosis 1999;19(9):813-6.
1999: Kumar A; Cassidy S B; Romero L; Schwartz S
Molecular cytogenetics of a de novo interstitial deletion of chromosome arm 6q in a developmentally normal girl.
American journal of medical genetics 1999;86(3):227-31.
1999: Kochera M; Depinet T W; Pretlow T P; Giaconia J M; Edgehouse N L; Pretlow T G; Schwartz S
Molecular cytogenetic studies of a serially transplanted primary prostatic carcinoma xenograft (CWR22) and four relapsed tumors.
The Prostate 1999;41(1):7-11.
1999: Amos-Landgraf J M; Ji Y; Gottlieb W; Depinet T; Wandstrat A E; Cassidy S B; Driscoll D J; Rogan P K; Schwartz S; Nicholls R D
Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints.
American journal of human genetics 1999;65(2):370-86.
1999: Wolf N G; Abdul-Karim F W; Farver C; Schröck E; du Manoir S; Schwartz S
Analysis of ovarian borderline tumors using comparative genomic hybridization and fluorescence in situ hybridization.
Genes, chromosomes & cancer 1999;25(4):307-15.
1999: Schwartz S
Molecular cytogenetics: show me the colors.
Genetics in medicine : official journal of the American College of Medical Genetics 1999;1(5):178-80.
1999: Sramkoski R M; Pretlow T G; Giaconia J M; Pretlow T P; Schwartz S; Sy M S; Marengo S R; Rhim J S; Zhang D; Jacobberger J W
A new human prostate carcinoma cell line, 22Rv1.
In vitro cellular & developmental biology. Animal 1999;35(7):403-9.
1999: Limwongse C; Schwartz S; Bocian M; Robin N H
Child with mosaic variegated aneuploidy and embryonal rhabdomyosarcoma.
American journal of medical genetics 1999;82(1):20-4.
1999: Siu I M; Robinson D R; Schwartz S; Kung H J; Pretlow T G; Petersen R B; Pretlow T P
The identification of monoclonality in human aberrant crypt foci.
Cancer research 1999;59(1):63-6.
1998: Zinn A R; Tonk V S; Chen Z; Flejter W L; Gardner H A; Guerra R; Kushner H; Schwartz S; Sybert V P; Van Dyke D L; Ross J L
Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1.
American journal of human genetics 1998;63(6):1757-66.
1998: Schumacher A; Lichtarge O; Schwartz S; Magnuson T
The murine Polycomb-group gene eed and its human orthologue: functional implications of evolutionary conservation.
Genomics 1998;54(1):79-88.
1998: Kumar A; Becker L A; Depinet T W; Haren J M; Kurtz C L; Robin N H; Cassidy S B; Wolff D J; Schwartz S
Molecular characterization and delineation of subtle deletions in de novo "balanced" chromosomal rearrangements.
Human genetics 1998;103(2):173-8.
1998: Eshleman J R; Casey G; Kochera M E; Sedwick W D; Swinler S E; Veigl M L; Willson J K; Schwartz S; Markowitz S D
Chromosome number and structure both are markedly stable in RER colorectal cancers and are not destabilized by mutation of p53.
Oncogene 1998;17(6):719-25.
1998: Wolff D J; Schwartz S; Montgomery T; Zackowski J L
Random X inactivation in a girl with a balanced t(X;9) and an abnormal phenotype.
American journal of medical genetics 1998;77(5):401-4.
1998: Fujimoto A; Lin M S; Schwartz S
Direct duplication of 9p22-->p24 in a child with duplication 9p syndrome.
American journal of medical genetics 1998;77(4):268-71.
1998: Dewald G; Stallard R; Al Saadi A; Arnold S; Bader P I; Blough R; Chen K; Elejalde B R; Harris C J; Higgins R R; Hoeltge G A; Hsu W T; Kubic V; McCorquodale D J; Micale M A; Moore J W; Phillips R M; Scheib-Wixted S; Schwartz S; Siembieda S; Strole K; VanTuinen P; Vance G H; Wiktor A; Zinsmeister A
A multicenter investigation with interphase fluorescence in situ hybridization using X- and Y-chromosome probes.
American journal of medical genetics 1998;76(4):318-26.
1998: Wandstrat A E; Leana-Cox J; Jenkins L; Schwartz S
Molecular cytogenetic evidence for a common breakpoint in the largest inverted duplications of chromosome 15.
American journal of human genetics 1998;62(4):925-36.
1998: Cassidy S B; Schwartz S
Prader-Willi and Angelman syndromes. Disorders of genomic imprinting.
Medicine 1998;77(2):140-51.
1998: Tsuchiya K D; Wiesner G; Cassidy S B; Limwongse C; Boyle J T; Schwartz S
Deletion 10q23.2-q23.33 in a patient with gastrointestinal juvenile polyposis and other features of a Cowden-like syndrome.
Genes, chromosomes & cancer 1998;21(2):113-8.
1997: Vance G H; Curtis C A; Heerema N A; Schwartz S; Palmer C G
An apparently acentric marker chromosome originating from 9p with a functional centromere without detectable alpha and beta satellite sequences.
American journal of medical genetics 1997;71(4):436-42.
1997: Crowe C A; Schwartz S; Black C J; Jaswaney V
Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes.
American journal of medical genetics 1997;71(4):406-13.
1997: Conroy J M; Grebe T A; Becker L A; Tsuchiya K; Nicholls R D; Buiting K; Horsthemke B; Cassidy S B; Schwartz S
Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndrome.
American journal of human genetics 1997;61(2):388-94.
1997: Robin N H; Harari-Shacham A; Schwartz S; Wolff D J
Duplication 14(q24.3q31) in a father and daughter: delineation of a possible imprinted region.
American journal of medical genetics 1997;71(3):361-5.
1997: Depinet T W; Zackowski J L; Earnshaw W C; Kaffe S; Sekhon G S; Stallard R; Sullivan B A; Vance G H; Van Dyke D L; Willard H F; Zinn A B; Schwartz S
Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA.
Human molecular genetics 1997;6(8):1195-204.
1997: Wolff D J; Gustashaw K M; Zurcher V; Ko L; White W; Weiss L; Van Dyke D L; Schwartz S; Willard H F
Deletions in Xq26.3-q27.3 including FMR1 result in a severe phenotype in a male and variable phenotypes in females depending upon the X inactivation pattern.
Human genetics 1997;100(2):256-61.
1997: Gunay-Aygun M; Heeger S; Schwartz S; Cassidy S B
Delayed diagnosis in patients with Prader-Willi syndrome due to maternal uniparental disomy 15.
American journal of medical genetics 1997;71(1):106-10.
1997: Schwartz S; Depinet T W; Leana-Cox J; Isada N B; Karson E M; Park V M; Pasztor L M; Sheppard L C; Stallard R; Wolff D J; Zinn A B; Zurcher V L; Zackowski J L
Sex chromosome markers: characterization using fluorescence in situ hybridization and review of the literature.
American journal of medical genetics 1997;71(1):1-7.
1997: Connerton-Moyer K J; Nicholls R D; Schwartz S; Driscoll D J; Hendrickson J E; Williams C A; Pauli R M
Unexpected familial recurrence in Angelman syndrome.
American journal of medical genetics 1997;70(3):253-60.
1997: McDaniel L D; Zhang B; Kubiczek E; Ritter M; Huang J; Berard C; Leana-Cox J; Schwartz S; Schultz R A
Construction and screening of a cosmid library generated from a somatic cell hybrid bearing human chromosome 15.
Genomics 1997;40(1):63-72.
1997: Cassidy S B; Forsythe M; Heeger S; Nicholls R D; Schork N; Benn P; Schwartz S
Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15.
American journal of medical genetics 1997;68(4):433-40.
1997: Saitoh S; Buiting K; Cassidy S B; Conroy J M; Driscoll D J; Gabriel J M; Gillessen-Kaesbach G; Glenn C C; Greenswag L R; Horsthemke B; Kondo I; Kuwajima K; Niikawa N; Rogan P K; Schwartz S; Seip J; Williams C A; Nicholls R D
Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation.
American journal of medical genetics 1997;68(2):195-206.
1996: Dewald G W; Stallard R; Bader P I; Chen K; Zenger-Hain J; Harris C J; Higgins R; Hirsch B; Hsu W T; Johnson E; Kubic V; Kurczynski T W; Malone J M; McCorquodale D J; Meilinger K; Meisner L F; Moore J W; Schwartz S; Siembieda S; Storto P D; Vance G; Van Tuinen P; Wiktor A; Yung J F
Toward quality assurance for metaphase FISH: a multicenter experience.
American journal of medical genetics 1996;65(3):190-6.
1996: Micale M A; Wolff D J; Dickerman L H; Redline R; Conroy J M; Schwartz S
Cytogenetic and molecular genetic characterization of trisomy 20 mosaicism in fetal blood and tissues.
Prenatal diagnosis 1996;16(10):893-7.
1996: Dewald G; Stallard R; Bader P I; Chen K; Zenger-Hain J; Harris C J; Higgins R; Hirsch B; Hsu W T; Johnson E; Kubic V; Kurczynski T W; Malone J M; McCorquodale D J; Meilinger K; Meisner L F; Moore J W; Schwartz S; Siembieda S; Storto P D; Vance G; Van Tuinen P; Wiktor A; Yung J F
Toward quality assurance for metaphase FISH: a multi-center experience.
American journal of medical genetics 1996;64(4):539-45.
1996: Wolf N G; Abdul-Karim F W; Schork N J; Schwartz S
Origins of heterogeneous ovarian carcinomas. A molecular cytogenetic analysis of histologically benign, low malignant potential, and fully malignant components.
The American journal of pathology 1996;149(2):511-20.
1996: Nagabhushan M; Miller C M; Pretlow T P; Giaconia J M; Edgehouse N L; Schwartz S; Kung H J; de Vere White R W; Gumerlock P H; Resnick M I; Amini S B; Pretlow T G
CWR22: the first human prostate cancer xenograft with strongly androgen-dependent and relapsed strains both in vivo and in soft agar.
Cancer research 1996;56(13):3042-6.
1996: Sullivan B A; Jenkins L S; Karson E M; Leana-Cox J; Schwartz S
Evidence for structural heterogeneity from molecular cytogenetic analysis of dicentric Robertsonian translocations.
American journal of human genetics 1996;59(1):167-75.
1996: Bolk S; Angrist M; Schwartz S; Silvestri J M; Weese-Mayer D E; Chakravarti A
Congenital central hypoventilation syndrome: mutation analysis of the receptor tyrosine kinase RET.
American journal of medical genetics 1996;63(4):603-9.
1996: Wolff D J; Miller A P; Van Dyke D L; Schwartz S; Willard H F
Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.
American journal of human genetics 1996;58(1):154-60.
1996: Sullivan B A; Schwartz S; Willard H F
Centromeres of human chromosomes.
Environmental and molecular mutagenesis 1996;28(3):182-91.
1995: Sullivan B A; Schwartz S
Identification of centromeric antigens in dicentric Robertsonian translocations: CENP-C and CENP-E are necessary components of functional centromeres.
Human molecular genetics 1995;4(12):2189-97.
1995: Sullivan B A; Schiffer C A; Patil S R; Hulseberg D; Leana-Cox J; Schwartz S
Application of FISH to complex chromosomal rearrangements associated with chronic myelogenous leukemia.
Cancer genetics and cytogenetics 1995;82(2):93-9.
1995: Micale M A; Haren J M; Conroy J M; Crowe C A; Schwartz S
Parental origin of De Novo chromosome 9 deletions in del(9p) syndrome.
American journal of medical genetics 1995;57(1):79-81.
1995: Stallard R; Krueger S; James R S; Schwartz S
Uniparental isodisomy 13 in a normal female due to transmission of a maternal t(13q13q).
American journal of medical genetics 1995;57(1):14-8.
1995: Buiting K; Saitoh S; Gross S; Dittrich B; Schwartz S; Nicholls R D; Horsthemke B
Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.
Nature genetics 1995;9(4):395-400.
1995: Lurie I W; Schwartz M F; Schwartz S; Cohen M M
Trisomy 7p resulting from isochromosome formation and whole-arm translocation.
American journal of medical genetics 1995;55(1):62-6.
1994: Sullivan B A; Wolff D J; Schwartz S
Analysis of centromeric activity in Robertsonian translocations: implications for a functional acrocentric hierarchy.
Chromosoma 1994;103(7):459-67.
1994: Wainstein M A; He F; Robinson D; Kung H J; Schwartz S; Giaconia J M; Edgehouse N L; Pretlow T P; Bodner D R; Kursh E D
CWR22: androgen-dependent xenograft model derived from a primary human prostatic carcinoma.
Cancer research 1994;54(23):6049-52.
1994: Baker P; Piven J; Schwartz S; Patil S
Brief report: duplication of chromosome 15q11-13 in two individuals with autistic disorder.
Journal of autism and developmental disorders 1994;24(4):529-35.
1994: Wolff D J; Brown C J; Schwartz S; Duncan A M; Surti U; Willard H F
Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations.
American journal of human genetics 1994;55(1):87-95.
1994: Prabhakar G; Schwartz S; Waters E; Punzalan C; Cohen M M
Complex karyotypic mosaicism as a result of non-disjunction and subsequent centromere fission.
Prenatal diagnosis 1994;14(7):595-8.
1994: Leana-Cox J; Jenkins L; Palmer C G; Plattner R; Sheppard L; Flejter W L; Zackowski J; Tsien F; Schwartz S
Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.
American journal of human genetics 1994;54(5):748-56.
1993: Rosenblum-Vos L S; Meltzer S J; Leana-Cox J; Schwartz S
Cytogenetic studies of primary cultures of esophageal squamous cell carcinoma.
Cancer genetics and cytogenetics 1993;70(2):127-31.
1993: Hoeltge G A; Dewald G; Palmer C G; David-Nelson M A; Saikevych I; Patil S; Schwartz S; Schneider N R; Herrmann M
Proficiency testing in clinical cytogenetics. A 6-year experience with photographs, fixed cells, and fresh blood.
Archives of pathology & laboratory medicine 1993;117(8):776-9.
1993: Schwartz S; Leana-Cox J
Fluorescent in situ hybridization (FISH): a new application in the delineation of true vs. pseudomosaicism in prenatal diagnosis.
Prenatal diagnosis 1993;13(8):661-70.
1993: Sullivan B A; Leana-Cox J; Schwartz S
Clarification of subtle reciprocal rearrangements using fluorescence in situ hybridization.
American journal of medical genetics 1993;47(2):223-30.
1993: Leana-Cox J; Levin S; Surana R; Wulfsberg E; Keene C L; Raffel L J; Sullivan B; Schwartz S
Characterization of de novo duplications in eight patients by using fluorescence in situ hybridization with chromosome-specific DNA libraries.
American journal of human genetics 1993;52(6):1067-73.
1993: Chase M B; Baek S J; Purtell D C; Schwartz S; Shen R F
Mapping of the human thromboxane synthase gene (TBXAS1) to chromosome 7q34-q35 by two-color fluorescence in situ hybridization.
Genomics 1993;16(3):771-3.
1993: Wolff D J; Schwartz M F; Cohen M M; Schwartz S
Precise mapping of a de novo duplication 18(q21-->q22) utilizing cytogenetic, biochemical, and molecular techniques.
American journal of medical genetics 1993;46(5):520-3.
1993: Wolff D J; Schwartz S
The effect of Robertsonian translocation on recombination on chromosome 21.
Human molecular genetics 1993;2(6):693-9.
1993: Schwartz S
Efficacy and applicability of interphase fluorescence in situ hybridization for prenatal diagnosis.
American journal of human genetics 1993;52(5):851-3.
1992: Schwartz S; Raffel L J
Prenatal detection of 45,X/46,XX/47,XXX mosaicism through amniocentesis: mosaicism confirmed in cord blood, amnion, and chorion.
Prenatal diagnosis 1992;12(12):1043-6.
1992: Saller D N; Canick J A; Schwartz S; Blitzer M G
Multiple-marker screening in pregnancies with hydropic and nonhydropic Turner syndrome.
American journal of obstetrics and gynecology 1992;167(4 Pt 1):1021-4.
1992: Schwartz S; Raffel L J; Sun C C; Waters E
An unusual mosaic karyotype detected through prenatal diagnosis with duplication of 1q and 19p and associated teratoma development.
Teratology 1992;46(4):399-404.
1992: Ripple M G; Goldberger B A; Caplan Y H; Blitzer M G; Schwartz S
Detection of cocaine and its metabolites in human amniotic fluid.
Journal of analytical toxicology 1992;16(5):328-31.
1992: Hogge W A; Hogge J S; Keene C L; Pupkin M; Schwartz S; McGillis C; Hartlove C; Crenshaw C; Cohen M M
Chorionic villus sampling: the University of Maryland experience.
Maryland medical journal (Baltimore, Md. : 1985) 1992;41(6):523-5.
1992: Wolff D J; Schwartz S
Characterization of Robertsonian translocations by using fluorescence in situ hybridization.
American journal of human genetics 1992;50(1):174-81.
1991: Wolff D J; Raffel L J; Ferré M M; Schwartz S
Prenatal ascertainment of an inherited dup(18p) associated with an apparently normal phenotype.
American journal of medical genetics 1991;41(3):319-21.
1991: Schwartz S; Harris M; Ehrenpreis R; Zaslav A; Raffel L J; Schwartz M F; Lieber E; Cohen M M
De novo 13q partial duplication identified by cytogenetic, biochemical and molecular approaches.
Clinical genetics 1991;40(6):417-22.
1991: Wolff D J; Needleman B W; Wasserman S S; Schwartz S
Spontaneous and clastogen induced chromosomal breakage in scleroderma.
The Journal of rheumatology 1991;18(6):837-40.
1991: Stephenson W P; Chute C G; Guess H A; Schwartz S; Lieber M
Incidence and outcome of surgery for benign prostatic hyperplasia among residents of Rochester, Minnesota: 1980-87. A population-based study.
Urology 1991;38(1 Suppl):32-42.
1990: Saller D N; Keene C L; Sun C C; Schwartz S
The association of single umbilical artery with cytogenetically abnormal pregnancies.
American journal of obstetrics and gynecology 1990;163(3):922-5.
1990: Roskes E J; Boughman J A; Schwartz S; Cohen M M
Congenital cardiovascular malformations (CCVM) and structural chromosome abnormalities: a report of 9 cases and literature review.
Clinical genetics 1990;38(3):198-210.
1990: Zackowski J L; Raffel L J; Blank C A; Schwartz S
Proximal interstitial deletion of 7q: a case report and review of the literature.
American journal of medical genetics 1990;36(3):328-32.
1990: Schwartz S; Astemborski J A; Budacz A P; Boughman J A; Wasserman S S; Cohen M M
Repeated measurement of spontaneous and clastogen-induced sister-chromatid exchange.
Mutation research 1990;234(2):51-9.
1990: Zackowski J L; Raffel L J; McDaniel L D; Schwartz S
A paternal balanced translocation [t(7;22)(q32;q13.3)] leading to reciprocal unbalanced karyotypes in two consecutive pregnancies.
Annales de génétique 1990;33(2):113-6.
1990: Wasserman S S; Cohen M M; Schwartz S
Factors underlying variation in spontaneous and clastogen-induced sister chromatid exchanges and chromosome breakage frequencies.
Environmental and molecular mutagenesis 1990;16(4):255-9.
1989: Day P; Shalaby Z; Cohen M M; Wasserman S S; Schwartz S
Effects of theophylline on chromosomal breakage and sister-chromatid exchange.
Mutation research 1989;224(4):409-13.
1989: Blitzer M G; Schwartz S; Cowan T M; Raffel L J
Recent advances in genetics.
Maryland medical journal (Baltimore, Md. : 1985) 1989;38(11):917-24.
1989: Schwartz S; Ashai S; Meijboom E J; Schwartz M F; Sun C C; Cohen M M
Prenatal detection of trisomy 9 mosaicism.
Prenatal diagnosis 1989;9(8):549-54.
1989: Cohen M M; Schwartz S; Schwartz M F; Blitzer M G; Raffel L J; Mullins-Keene C L; Sun C C; Blakemore K J
Antenatal detection of cystic hygroma.
Obstetrical & gynecological survey 1989;44(6):481-90.
1989: Schwartz S; Roulston D; Cohen M M
dNORs and meiotic nondisjunction.
American journal of human genetics 1989;44(5):627-30.
1989: Roulston D; Antonarakis S E; Lewis J G; Cohen M M; Schwartz S
Cytological and molecular studies of nucleolar organizing region variants and recombination in trisomy 21.
Progress in clinical and biological research 1989;311():81-100.
1988: Cohen M M; Schwartz S; Kunska A; Satish J; Hamburger A
The effect of tissue culture agar on chromosome breakage, sister-chromatid exchanges and clonogenicity in human cells.
Mutation research 1988;208(3-4):201-5.
1986: Schwartz S; Schwartz M F; Panny S R; Peterson C J; Waters E; Cohen M M
Inherited X-chromosome inverted tandem duplication in a male traced to a grandparental mitotic error.
American journal of human genetics 1986;38(5):741-50.
1986: Schwartz S; Jiji R; Meekins J; Cohen M M
Chromosome abnormalities in acquired idiopathic sideroblastic anemia with subsequent leukemic transformation.
Cancer genetics and cytogenetics 1986;19(3-4):291-9.
1986: Boughman J A; Halloran S L; Roulston D; Schwartz S; Suzuki J B; Weitkamp L R; Wenk R E; Wooten R; Cohen M M
An autosomal-dominant form of juvenile periodontitis: its localization to chromosome 4 and linkage to dentinogenesis imperfecta and Gc.
Journal of craniofacial genetics and developmental biology 1986;6(4):341-50.
1986: Schwartz S; Palmer C G; Yu P L; Boughman J A; Cohen M M
Analysis of translocations observed in three different populations. II. Robertsonian translocations.
Cytogenetics and cell genetics 1986;42(1-2):53-6.
1986: Schwartz S; Palmer C G; Yu P L; Boughman J A; Cohen M M
Analysis of translocations observed in three different populations. I. Reciprocal translocations.
Cytogenetics and cell genetics 1986;42(1-2):42-52.
1985: Schwartz M; Schwartz S; Wenk R E; Cohen M
Amniotic fluid and advances in prenatal diagnosis.
Clinics in laboratory medicine 1985;5(2):371-87.
1985: Pearson M G; Vardiman J W; Le Beau M M; Rowley J D; Schwartz S; Kerman S L; Cohen M M; Fleischman E W; Prigogina E L
Increased numbers of marrow basophils may be associated with a t(6;9) in ANLL.
American journal of hematology 1985;18(4):393-403.
1985: Schwartz S; Beisel J H; Panny S R; Cohen M M
A complex rearrangement, including a deleted 8q, in a case of Langer-Giedion syndrome.
Clinical genetics 1985;27(2):175-82.
1985: Schwartz S; Max S R; Panny S R; Cohen M M
Deletions of proximal 15q and non-classical Prader-Willi syndrome phenotypes.
American journal of medical genetics 1985;20(2):255-63.
1985: Schwartz S; Flannery D B; Cohen M M
Tests appropriate for the prenatal diagnosis of ataxia telangiectasia.
Prenatal diagnosis 1985;5(1):9-14.
1984: Schwartz S; Palmer C G
High-resolution chromosome analysis: I. Applications and limitations.
American journal of medical genetics 1984;19(2):291-9.
1984: Schwartz S; Cohen M M; Panny S R; Beisel J H; Vora S
Duplication of chromosome 10p: confirmation of regional assignments of platelet-type phosphofructokinase.
American journal of human genetics 1984;36(4):750-9.
1983: Schwartz S; Jiji R; Kerman S; Meekins J; Cohen M M
Translocation (6;9)(p23;q34) in acute nonlymphocytic leukemia.
Cancer genetics and cytogenetics 1983;10(2):133-8.
1983: Schwartz S; Meekins J; Panny S R; Sun C C; Cohen M M
Brief clinical report: cebocephaly-holoprosencephaly in a newborn girl with a terminal 7q deletion [46,XX,del(7)(pter leads to q32:)].
American journal of medical genetics 1983;15(1):141-4.
1983: Schwartz S; Palmer C G; Weaver D D; Priest J
Dicentric chromosome 13 and centromere inactivation.
Human genetics 1983;63(4):332-7.
1983: Schwartz S; Palmer C G
Chromosomal findings in 164 couples with repeated spontaneous abortions: with special consideration to prior reproductive history.
Human genetics 1983;63(1):28-34.
1961: COHEN M M; WINER R A; SCHWARTZ S; SHKLAR G
Oral aspects of mongolism. I. Periodontal disease in mongolism.
Oral surgery, oral medicine, and oral pathology 1961;14():92-107.

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