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Terry Hassold

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Hunt Patricia A; Susiarjo Martha; Rubio Carmen; Hassold Terry J
The bisphenol A experience: a primer for the analysis of environmental effects on mammalian reproduction.
Cheng Edith Y; Hunt Patricia A; Naluai-Cecchini Theresa A; Fligner Corrine L; Fujimoto Victor Y; Pasternack Tanya L; Schwartz Jackie M; Steinauer Jody E; Woodruff Tracey J; Cherry Sheila M; Hansen Terah A; Vallente Rhea U; Broman Karl W; Hassold Terry J
Meiotic recombination in human oocytes.
Hassold T; Hansen T; Hunt P; VandeVoort C
Cytological studies of recombination in rhesus males.

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All Publications

2009: Hunt Patricia A; Susiarjo Martha; Rubio Carmen; Hassold Terry J
The bisphenol A experience: a primer for the analysis of environmental effects on mammalian reproduction.
Biology of reproduction 2009;81(5):807-13.
2009: Cheng Edith Y; Hunt Patricia A; Naluai-Cecchini Theresa A; Fligner Corrine L; Fujimoto Victor Y; Pasternack Tanya L; Schwartz Jackie M; Steinauer Jody E; Woodruff Tracey J; Cherry Sheila M; Hansen Terah A; Vallente Rhea U; Broman Karl W; Hassold Terry J
Meiotic recombination in human oocytes.
PLoS genetics 2009;5(9):e1000661.
2009: Hassold T; Hansen T; Hunt P; VandeVoort C
Cytological studies of recombination in rhesus males.
Cytogenetic and genome research 2009;124(2):132-8.
2008: Anderson Ericka L; Baltus Andrew E; Roepers-Gajadien Hermien L; Hassold Terry J; de Rooij Dirk G; van Pelt Ans M M; Page David C
Stra8 and its inducer, retinoic acid, regulate meiotic initiation in both spermatogenesis and oogenesis in mice.
Proceedings of the National Academy of Sciences of the United States of America 2008;105(39):14976-80.
2008: Sanderson Matthew L; Hassold Terry J; Carrell Douglas T
Proteins involved in meiotic recombination: a role in male infertility?
Systems biology in reproductive medicine 2008;54(2):57-74.
2008: Hunt Patricia A; Hassold Terry J
Human female meiosis: what makes a good egg go bad?
Trends in genetics : TIG 2008;24(2):86-93.
2007: Hassold Terry; Hall Heather; Hunt Patricia
The origin of human aneuploidy: where we have been, where we are going.
Human molecular genetics 2007;16 Spec No. 2():R203-8.
2007: Hassold Terry; Hunt Patricia
Rescuing distal crossovers.
Nature genetics 2007;39(10):1187-8.
2007: Hall Heather E; Chan E Ricky; Collins Andrew; Judis LuAnn; Shirley Sofia; Surti Urvashi; Hoffner Lori; Cockwell Annette E; Jacobs Patricia A; Hassold Terry J
The origin of trisomy 13.
American journal of medical genetics. Part A 2007;143A(19):2242-8.
2007: Hall Heather E; Surti Urvashi; Hoffner Lori; Shirley Sofia; Feingold Eleanor; Hassold Terry
The origin of trisomy 22: evidence for acrocentric chromosome-specific patterns of nondisjunction.
American journal of medical genetics. Part A 2007;143A(19):2249-55.
2007: Cherry Sheila M; Adelman Carrie A; Theunissen Jan W; Hassold Terry J; Hunt Patricia A; Petrini John H J
The Mre11 complex influences DNA repair, synapsis, and crossing over in murine meiosis.
Current biology : CB 2007;17(4):373-8.
2007: Susiarjo Martha; Hassold Terry J; Freeman Edward; Hunt Patricia A
Bisphenol A exposure in utero disrupts early oogenesis in the mouse.
PLoS genetics 2007;3(1):e5.
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: Koehler Kara E; Schrump Stefanie E; Cherry Jonathan P; Hassold Terry J; Hunt Patricia A
Near-human aneuploidy levels in female mice with homeologous chromosomes.
Current biology : CB 2006;16(15):R579-80.
2006: Hall Heather; Hunt Patricia; Hassold Terry
Meiosis and sex chromosome aneuploidy: how meiotic errors cause aneuploidy; how aneuploidy causes meiotic errors.
Current opinion in genetics & development 2006;16(3):323-9.
2006: Vallente Rhea U; Cheng Edith Y; Hassold Terry J
The synaptonemal complex and meiotic recombination in humans: new approaches to old questions.
Chromosoma 2006;115(3):241-9.
2005: Hodges Craig A; Revenkova Ekaterina; Jessberger Rolf; Hassold Terry J; Hunt Patricia A
SMC1beta-deficient female mice provide evidence that cohesins are a missing link in age-related nondisjunction.
Nature genetics 2005;37(12):1351-5.
2005: Lynn Audrey; Schrump Stefanie; Cherry Jonathan; Hassold Terry; Hunt Patricia
Sex, not genotype, determines recombination levels in mice.
American journal of human genetics 2005;77(4):670-5.
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: Mann Michael B; Hodges Craig A; Barnes Ellen; Vogel Hannes; Hassold Terry J; Luo Guangbin
Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome.
Human molecular genetics 2005;14(6):813-25.
2005: Lamb N E; Sherman S L; Hassold T J
Effect of meiotic recombination on the production of aneuploid gametes in humans.
Cytogenetic and genome research 2005;111(3-4):250-5.
2004: Cherry Sheila M; Hunt Patricia A; Hassold Terry J
Cisplatin disrupts mammalian spermatogenesis, but does not affect recombination or chromosome segregation.
Mutation research 2004;564(2):115-28.
2004: Lamb Neil E; Hassold Terry J
Nondisjunction--a view from ringside.
The New England journal of medicine 2004;351(19):1931-4.
2004: Koehler Kara E; Millie Elise A; Cherry Jonathan P; Schrump Stefanie E; Hassold Terry J
Meiotic exchange and segregation in female mice heterozygous for paracentric inversions.
Genetics 2004;166(3):1199-214.
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: Lynn Audrey; Ashley Terry; Hassold Terry
Variation in human meiotic recombination.
Annual review of genomics and human genetics 2004;5():317-49.
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: Simpson Joe Leigh; de la Cruz Felix; Swerdloff Ronald S; Samango-Sprouse Carole; Skakkebaek Niels E; Graham John M; Hassold Terry; Aylstock Melissa; Meyer-Bahlburg Heino F L; Willard Huntington F; Hall Judith G; Salameh Wael; Boone Kyle; Staessen Catherine; Geschwind Dan; Giedd Jay; Dobs Adrian S; Rogol Alan; Brinton Bonnie; Paulsen C Alvin
Klinefelter syndrome: expanding the phenotype and identifying new research directions.
Genetics in medicine : official journal of the American College of Medical Genetics 2003;5(6):460-8.
2003: Hunt Patricia A; Koehler Kara E; Susiarjo Martha; Hodges Craig A; Ilagan Arlene; Voigt Robert C; Thomas Sally; Thomas Brian F; Hassold Terry J
Bisphenol a exposure causes meiotic aneuploidy in the female mouse.
Current biology : CB 2003;13(7):546-53.
2002: Koehler Kara E; Millie Elise A; Cherry Jonathan P; Burgoyne Paul S; Evans Edward P; Hunt Patricia A; Hassold Terry J
Sex-specific differences in meiotic chromosome segregation revealed by dicentric bridge resolution in mice.
Genetics 2002;162(3):1367-79.
2002: Koehler Kara E; Cherry Jonathan P; Lynn Audrey; Hunt Patricia A; Hassold Terry J
Genetic control of mammalian meiotic recombination. I. Variation in exchange frequencies among males from inbred mouse strains.
Genetics 2002;162(1):297-306.
2002: Bean Christopher J; Hassold Terry J; Judis LuAnn; Hunt Patricia A
Fertilization in vitro increases non-disjunction during early cleavage divisions in a mouse model system.
Human reproduction (Oxford, England) 2002;17(9):2362-7.
2002: Hunt Patricia A; Hassold Terry J
Sex matters in meiosis.
Science (New York, N.Y.) 2002;296(5576):2181-3.
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.
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: Bean C J; Hunt P A; Millie E A; Hassold T J
Analysis of a malsegregating mouse Y chromosome: evidence that the earliest cleavage divisions of the mammalian embryo are non-disjunction-prone.
Human molecular genetics 2001;10(9):963-72.
2001: Hassold T; Hunt P
To err (meiotically) is human: the genesis of human aneuploidy.
Nature reviews. Genetics 2001;2(4):280-91.
2000: Hixon M L; Obejero-Paz C; Muro-Cacho C; Wagner M W; Millie E; Nagy J; Hassold T J; Gualberto A
Cks1 mediates vascular smooth muscle cell polyploidization.
The Journal of biological chemistry 2000;275(51):40434-42.
2000: Hixon M L; Muro-Cacho C; Wagner M W; Obejero-Paz C; Millie E; Fujio Y; Kureishi Y; Hassold T; Walsh K; Gualberto A
Akt1/PKB upregulation leads to vascular smooth muscle cell hypertrophy and polyploidization.
The Journal of clinical investigation 2000;106(8):1011-20.
2000: Hassold T; Sherman S; Hunt P
Counting cross-overs: characterizing meiotic recombination in mammals.
Human molecular genetics 2000;9(16):2409-19.
2000: LePage D F; Church D M; Millie E; Hassold T J; Conlon R A
Rapid generation of nested chromosomal deletions on mouse chromosome 2.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(19):10471-6.
2000: Zaragoza M V; Surti U; Redline R W; Millie E; Chakravarti A; Hassold T J
Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform mole.
American journal of human genetics 2000;66(6):1807-20.
2000: Hassold T; Sherman S
Down syndrome: genetic recombination and the origin of the extra chromosome 21.
Clinical genetics 2000;57(2):95-100.
1999: Padungtod C; Hassold T J; Millie E; Ryan L M; Savitz D A; Christiani D C; Xu X
Sperm aneuploidy among Chinese pesticide factory workers: scoring by the FISH method.
American journal of industrial medicine 1999;36(2):230-8.
1999: Mroz K; Hassold T J; Hunt P A
Meiotic aneuploidy in the XXY mouse: evidence that a compromised testicular environment increases the incidence of meiotic errors.
Human reproduction (Oxford, England) 1999;14(5):1151-6.
1999: Yang Q; Sherman S L; Hassold T J; Allran K; Taft L; Pettay D; Khoury M J; Erickson J D; Freeman S B
Risk factors for trisomy 21: maternal cigarette smoking and oral contraceptive use in a population-based case-control study.
Genetics in medicine : official journal of the American College of Medical Genetics 1999;1(3):80-8.
1999: Redline R W; Zaragoza M; Hassold T
Prevalence of developmental and inflammatory lesions in nonmolar first-trimester spontaneous abortions.
Human pathology 1999;30(1):93-100.
1998: Hixon M; Millie E; Judis L A; Sherman S; Allran K; Taft L; Hassold T
FISH studies of the sperm of fathers of paternally derived cases of trisomy 21: no evidence for an increase in aneuploidy.
Human genetics 1998;103(6):654-7.
1998: Koehler K E; Hassold T J
Human aneuploidy: lessons from achiasmate segregation in Drosophila melanogaster.
Annals of human genetics 1998;62(Pt 6):467-79.
1998: Freeman S B; Taft L F; Dooley K J; Allran K; Sherman S L; Hassold T J; Khoury M J; Saker D M
Population-based study of congenital heart defects in Down syndrome.
American journal of medical genetics 1998;80(3):213-7.
1998: Zaragoza M V; Millie E; Redline R W; Hassold T J
Studies of non-disjunction in trisomies 2, 7, 15, and 22: does the parental origin of trisomy influence placental morphology?
Journal of medical genetics 1998;35(11):924-31.
1998: Shaffer L G; McCaskill C; Adkins K; Hassold T J
Systematic search for uniparental disomy in early fetal losses: the results and a review of the literature.
American journal of medical genetics 1998;79(5):366-72.
1998: Redline R W; Hassold T; Zaragoza M
Determinants of villous trophoblastic hyperplasia in spontaneous abortions.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 1998;11(8):762-8.
1998: Savage A R; Petersen M B; Pettay D; Taft L; Allran K; Freeman S B; Karadima G; Avramopoulos D; Torfs C; Mikkelsen M; Hassold T J; Sherman S L
Elucidating the mechanisms of paternal non-disjunction of chromosome 21 in humans.
Human molecular genetics 1998;7(8):1221-7.
1998: Shen J J; Sherman S L; Hassold T J
Centromeric genotyping and direct analysis of nondisjunction in humans: Down syndrome.
Chromosoma 1998;107(3):166-72.
1998: Redline R W; Hassold T; Zaragoza M V
Prevalence of the partial molar phenotype in triploidy of maternal and paternal origin.
Human pathology 1998;29(5):505-11.
1998: Hassold T J
Nondisjunction in the human male.
Current topics in developmental biology 1998;37():383-406.
1997: O'Keefe C L; Griffin D K; Bean C J; Matera A G; Hassold T J
Alphoid variant-specific FISH probes can distinguish autosomal meiosis I from meiosis II non-disjunction in human sperm.
Human genetics 1997;101(1):61-6.
1997: Griffin D K; Millie E A; Redline R W; Hassold T J; Zaragoza M V
Cytogenetic analysis of spontaneous abortions: comparison of techniques and assessment of the incidence of confined placental mosaicism.
American journal of medical genetics 1997;72(3):297-301.
1997: Lamb N E; Feingold E; Savage A; Avramopoulos D; Freeman S; Gu Y; Hallberg A; Hersey J; Karadima G; Pettay D; Saker D; Shen J; Taft L; Mikkelsen M; Petersen M B; Hassold T; Sherman S L
Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21.
Human molecular genetics 1997;6(9):1391-9.
1997: Zaragoza M V; Keep D; Genest D R; Hassold T; Redline R W
Early complete hydatidiform moles contain inner cell mass derivatives.
American journal of medical genetics 1997;70(3):273-7.
1996: Lamb N E; Freeman S B; Savage-Austin A; Pettay D; Taft L; Hersey J; Gu Y; Shen J; Saker D; May K M; Avramopoulos D; Petersen M B; Hallberg A; Mikkelsen M; Hassold T J; Sherman S L
Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II.
Nature genetics 1996;14(4):400-5.
1996: Griffin D K; Abruzzo M A; Millie E A; Feingold E; Hassold T J
Sex ratio in normal and disomic sperm: evidence that the extra chromosome 21 preferentially segregates with the Y chromosome.
American journal of human genetics 1996;59(5):1108-13.
1996: Keep D; Zaragoza M V; Hassold T; Redline R W
Very early complete hydatidiform mole.
Human pathology 1996;27(7):708-13.
1996: Abruzzo M A; Griffin D K; Millie E A; Sheean L A; Hassold T J
The effect of Y-chromosome alpha-satellite array length on the rate of sex chromosome disomy in human sperm.
Human genetics 1996;97(6):819-23.
1996: Yoon P W; Freeman S B; Sherman S L; Taft L F; Gu Y; Pettay D; Flanders W D; Khoury M J; Hassold T J
Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study.
American journal of human genetics 1996;58(3):628-33.
1996: Hassold T; Abruzzo M; Adkins K; Griffin D; Merrill M; Millie E; Saker D; Shen J; Zaragoza M
Human aneuploidy: incidence, origin, and etiology.
Environmental and molecular mutagenesis 1996;28(3):167-75.
1995: Griffin D K; Abruzzo M A; Millie E A; Sheean L A; Feingold E; Sherman S L; Hassold T J
Non-disjunction in human sperm: evidence for an effect of increasing paternal age.
Human molecular genetics 1995;4(12):2227-32.
1995: Hassold T; Merrill M; Adkins K; Freeman S; Sherman S
Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16.
American journal of human genetics 1995;57(4):867-74.
1995: Shen J J; Williams B J; Zipursky A; Doyle J; Sherman S L; Jacobs P A; Shugar A L; Soukup S W; Hassold T J
Cytogenetic and molecular studies of Down syndrome individuals with leukemia.
American journal of human genetics 1995;56(4):915-25.
1995: Hassold T; Sherman S; Hunt P A
The origin of trisomy in humans.
Progress in clinical and biological research 1995;393():1-12.
1995: Abruzzo M A; Hassold T J
Etiology of nondisjunction in humans.
Environmental and molecular mutagenesis 1995;25 Suppl 26():38-47.
1995: Jacobs P A; Hassold T J
The origin of numerical chromosome abnormalities.
Advances in genetics 1995;33():101-33.
1994: Zaragoza M V; Jacobs P A; James R S; Rogan P; Sherman S; Hassold T
Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns.
Human genetics 1994;94(4):411-7.
1994: Sherman S L; Petersen M B; Freeman S B; Hersey J; Pettay D; Taft L; Frantzen M; Mikkelsen M; Hassold T J
Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination.
Human molecular genetics 1994;3(9):1529-35.
1994: MacDonald M; Hassold T; Harvey J; Wang L H; Morton N E; Jacobs P
The origin of 47,XXY and 47,XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination.
Human molecular genetics 1994;3(8):1365-71.
1994: James R S; Temple I K; Patch C; Thompson E M; Hassold T; Jacobs P A
A systematic search for uniparental disomy in carriers of chromosome translocations.
European journal of human genetics : EJHG 1994;2(2):83-95.
1993: Williams B J; Ballenger C A; Malter H E; Bishop F; Tucker M; Zwingman T A; Hassold T J
Non-disjunction in human sperm: results of fluorescence in situ hybridization studies using two and three probes.
Human molecular genetics 1993;2(11):1929-36.
1993: Petersen M B; Antonarakis S E; Hassold T J; Freeman S B; Sherman S L; Avramopoulos D; Mikkelsen M
Paternal nondisjunction in trisomy 21: excess of male patients.
Human molecular genetics 1993;2(10):1691-5.
1993: Hassold T; Hunt P A; Sherman S
Trisomy in humans: incidence, origin and etiology.
Current opinion in genetics & development 1993;3(3):398-403.
1993: Freeman S B; May K M; Pettay D; Fernhoff P M; Hassold T J
Paternal uniparental disomy in a child with a balanced 15;15 translocation and Angelman syndrome.
American journal of medical genetics 1993;45(5):625-30.
1992: Lorber B J; Grantham M; Peters J; Willard H F; Hassold T J
Nondisjunction of chromosome 21: comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin.
American journal of human genetics 1992;51(6):1265-76.
1992: Takaesu N; Newfeld S; Hassold T
Characterization of three VNTR systems at D21S112.
Genomics 1992;14(3):816-7.
1992: Hassold T; Pettay D; Robinson A; Uchida I
Molecular studies of parental origin and mosaicism in 45,X conceptuses.
Human genetics 1992;89(6):647-52.
1992: Krasikov N; Takaesu N; Hassold T; Knops J F; Finley W H; Scarbrough P
Molecular and cytogenetic investigation of complex tissue-specific duplication and loss of chromosome 21 in a child with a monosomy 21 phenotype.
American journal of medical genetics 1992;43(3):554-60.
1991: Hassold T J; Sherman S L; Pettay D; Page D C; Jacobs P A
XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region.
American journal of human genetics 1991;49(2):253-60.
1991: Temple I K; Cockwell A; Hassold T; Pettay D; Jacobs P
Maternal uniparental disomy for chromosome 14.
Journal of medical genetics 1991;28(8):511-4.
1991: Hassold T J; Pettay D; Freeman S B; Grantham M; Takaesu N
Molecular studies of non-disjunction in trisomy 16.
Journal of medical genetics 1991;28(3):159-62.
1990: Hassold T; Pettay D; May K; Robinson A
Analysis of non-disjunction in sex chromosome tetrasomy and pentasomy.
Human genetics 1990;85(6):648-50.
1990: May K M; Jacobs P A; Lee M; Ratcliffe S; Robinson A; Nielsen J; Hassold T J
The parental origin of the extra X chromosome in 47,XXX females.
American journal of human genetics 1990;46(4):754-61.
1990: Morton N E; Keats B J; Jacobs P A; Hassold T; Pettay D; Harvey J; Andrews V
A centromere map of the X chromosome from trisomies of maternal origin.
Annals of human genetics 1990;54(Pt 1):39-47.
1990: Harvey J; Jacobs P A; Hassold T; Pettay D
The parental origin of 47,XXY males.
Birth defects original article series 1990;26(4):289-96.
1990: Hassold T; Arnovitz K; Jacobs P A; May K; Robinson D
The parental origin of the missing or additional chromosome in 45,X and 47,XXX females.
Birth defects original article series 1990;26(4):297-304.
1990: Takaesu N; Jacobs P A; Cockwell A; Blackston R D; Freeman S; Nuccio J; Kurnit D M; Uchida I; Freeman V; Hassold T
Nondisjunction of chromosome 21.
American journal of medical genetics. Supplement 1990;7():175-81.
1989: Hassold T J; Takaesu N
Analysis of non-disjunction in human trisomic spontaneous abortions.
Progress in clinical and biological research 1989;311():115-34.
1989: Buraczynska M; Stewart G D; Sherman S; Freeman V; Grantham M; Uchida I; Hassold T; Kurnit D M
Studying nondisjunction of chromosome 21 with cytogenetic markers on the short arm and DNA markers encompassing the long arm.
Progress in clinical and biological research 1989;311():101-13.
1989: Jacobs P; Hassold T; Harvey J; May K
The origin of sex chromosome aneuploidy.
Progress in clinical and biological research 1989;311():135-51.
1988: Jacobs P A; Hassold T J; Whittington E; Butler G; Collyer S; Keston M; Lee M
Klinefelter's syndrome: an analysis of the origin of the additional sex chromosome using molecular probes.
Annals of human genetics 1988;52(Pt 2):93-109.
1988: Hassold T; Benham F; Leppert M
Cytogenetic and molecular analysis of sex-chromosome monosomy.
American journal of human genetics 1988;42(4):534-41.
1988: Stewart G D; Hassold T J; Berg A; Watkins P; Tanzi R; Kurnit D M
Trisomy 21 (Down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21.
American journal of human genetics 1988;42(2):227-36.
1988: Hassold T; Jacobs P A; Pettay D
Cytogenetic studies of couples with repeated spontaneous abortions of known karyotype.
Genetic epidemiology 1988;5(2):65-74.
1988: Stewart G D; Hassold T J; Kurnit D M
Trisomy 21. Molecular and cytogenetic studies of nondisjunction.
Advances in human genetics 1988;17():99-140.
1988: Harbison M; Hassold T; Kobryn C; Jacobs P A
Molecular studies of the parental origin and nature of human X isochromosomes.
Cytogenetics and cell genetics 1988;47(4):217-22.
1987: Jacobs P A; Hassold T J; Henry A; Pettay D; Takaesu N
Trisomy 13 ascertained in a survey of spontaneous abortions.
Journal of medical genetics 1987;24(12):721-4.
1987: Hassold T; Jacobs P A; Leppert M; Sheldon M
Cytogenetic and molecular studies of trisomy 13.
Journal of medical genetics 1987;24(12):725-32.
1987: Hassold T; Jacobs P A; Pettay D
Analysis of nucleolar organizing regions in parents of trisomic spontaneous abortions.
Human genetics 1987;76(4):381-4.
1985: Hassold T; Kumlin E; Takaesu N; Leppert M
Determination of the parental origin of sex-chromosome monosomy using restriction fragment length polymorphisms.
American journal of human genetics 1985;37(5):965-72.
1985: Hassold T; Kumlin E; Takaesu N; Leppert M
Use of restriction fragment length polymorphisms to study the origin of human aneuploidy.
Annals of the New York Academy of Sciences 1985;450():179-89.

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