Heike Starke

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Erlecke Jörn; Hartmann Isabell; Hoffmann Martin; Kroll Torsten; Starke Heike; Heller Anita; Gloria Alexander; Sayer Herbert G; Johannes Tilman; Claussen Uwe; Liehr Thomas; Loncarevic Ivan F
Automated detection of residual cells after sex-mismatched stem-cell transplantation - evidence for presence of disease-marker negative residual cells.
Santos Mònica; Mrasek Kristin; Rigola Maria Angels; Starke Heike; Liehr Thomas; Fuster Carme
Identification of a "cryptic mosaicism" involving at least four different small supernumerary marker chromosomes derived from chromosome 9 in a woman without reproductive success.
Fickelscher Ina; Starke Heike; Schulze Eberhard; Ernst Günther; Kosyakova Nadezda; Mkrtchyan Hasmik; MacDermont Kay; Sebire Neil; Liehr Thomas
A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1--evidence for high variability in mosaicism in different tissues of sSMC carriers.

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2009: Erlecke Jörn; Hartmann Isabell; Hoffmann Martin; Kroll Torsten; Starke Heike; Heller Anita; Gloria Alexander; Sayer Herbert G; Johannes Tilman; Claussen Uwe; Liehr Thomas; Loncarevic Ivan F
Automated detection of residual cells after sex-mismatched stem-cell transplantation - evidence for presence of disease-marker negative residual cells.
Molecular Cytogenetics 2009;2():12.
2007: Santos Mònica; Mrasek Kristin; Rigola Maria Angels; Starke Heike; Liehr Thomas; Fuster Carme
Identification of a "cryptic mosaicism" involving at least four different small supernumerary marker chromosomes derived from chromosome 9 in a woman without reproductive success.
Fertility and sterility 2007;88(4):969.e11-7.
2007: Fickelscher Ina; Starke Heike; Schulze Eberhard; Ernst Günther; Kosyakova Nadezda; Mkrtchyan Hasmik; MacDermont Kay; Sebire Neil; Liehr Thomas
A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1--evidence for high variability in mosaicism in different tissues of sSMC carriers.
Prenatal diagnosis 2007;27(8):783-5.
2007: Bartels Iris; Starke Heike; Argyriou Loukas; Sauter Simone M; Zoll Barbara; Liehr Thomas
An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype.
European journal of medical genetics 2007;50(2):133-8.
2007: Sun F; Oliver-Bonet M; Liehr T; Starke H; Ko E; Rademaker A; Martin R H
Discontinuities and unsynapsed regions in meiotic chromosomes have a trans effect on meiotic recombination of some chromosomes in human males.
Cytogenetic and genome research 2007;119(1-2):27-32.
2007: Backx L; Van Esch H; Melotte C; Kosyakova N; Starke H; Frijns J-P; Liehr T; Vermeesch J R
Array painting using microdissected chromosomes to map chromosomal breakpoints.
Cytogenetic and genome research 2007;116(3):158-66.
2006: Sun Fei; Oliver-Bonet M; Liehr T; Starke H; Turek P; Ko E; Rademaker A; Martin R H
Analysis of non-crossover bivalents in pachytene cells from 10 normal men.
Human reproduction (Oxford, England) 2006;21(9):2335-9.
2006: Sun Fei; Oliver-Bonet Maria; Liehr Thomas; Starke Heike; Turek Paul; Ko Evelyn; Rademaker Alfred; Martin Renée H
Variation in MLH1 distribution in recombination maps for individual chromosomes from human males.
Human molecular genetics 2006;15(15):2376-91.
2006: Liehr Thomas; Gross Madeleine; Karst Constanze; Glaser Melanie; Mrasek Kristin; Starke Heike; Weise Anja; Mkrtchyan Hasmik; Kuechler Alma
FISH banding in tumor cytogenetics.
Cancer genetics and cytogenetics 2006;164(1):88-9.
2006: Liehr Thomas; Starke Heike; Senger Gabriele; Melotte Cindy; Weise Anja; Vermeesch Joris Robert
Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC.
American journal of medical genetics. Part A 2006;140(1):46-51.
2006: Barber J C K; Zhang S; Friend N; Collins A L; Maloney V K; Hastings R; Farren B; Barnicoat A; Polityko A D; Rumyantseva N V; Starke H; Ye S
Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect.
Cytogenetic and genome research 2006;114(3-4):351-8.
2006: Dufke A; Singer S; Borell-Kost S; Stotter M; Pflumm D A; Mau-Holzmann U A; Starke H; Mrasek K; Enders H
De novostructural chromosomal imbalances: molecular cytogenetic characterization of partial trisomies.
Cytogenetic and genome research 2006;114(3-4):342-50.
2006: Brecevic L; Michel S; Starke H; Müller K; Kosyakova N; Mrasek K; Weise A; Liehr T
Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines.
Cytogenetic and genome research 2006;114(3-4):319-24.
2006: Liehr T; Starke H; Heller A; Kosyakova N; Mrasek K; Gross M; Karst C; Steinhaeuser U; Hunstig F; Fickelscher I; Kuechler A; Trifonov V; Romanenko S A; Weise A
Multicolor fluorescence in situ hybridization (FISH) applied to FISH-banding.
Cytogenetic and genome research 2006;114(3-4):240-4.
2006: Gross M; Starke H; Trifonov V; Claussen U; Liehr T; Weise A
A molecular cytogenetic study of chromosome evolution in chimpanzee.
Cytogenetic and genome research 2006;112(1-2):67-75.
2006: Liehr T; Mrasek K; Weise A; Dufke A; Rodríguez L; Martínez Guardia N; Sanchís A; Vermeesch J R; Ramel C; Polityko A; Haas O A; Anderson J; Claussen U; von Eggeling F; Starke H
Small supernumerary marker chromosomes--progress towards a genotype-phenotype correlation.
Cytogenetic and genome research 2006;112(1-2):23-34.
2005: Gutiérrez-Mateo C; Benet J; Starke H; Oliver-Bonet M; Munné S; Liehr T; Navarro J
Karyotyping of human oocytes by cenM-FISH, a new 24-colour centromere-specific technique.
Human reproduction (Oxford, England) 2005;20(12):3395-401.
2005: Sun Fei; Oliver-Bonet Maria; Liehr Thomas; Starke Heike; Trpkov Kiril; Ko Evelyn; Rademaker Alfred; Martin Renée H
Discontinuities and unsynapsed regions in meiotic chromosomes have a cis effect on meiotic recombination patterns in normal human males.
Human molecular genetics 2005;14(20):3013-8.
2005: von Beust G; Sauter S M; Liehr T; Burfeind P; Bartels I; Starke H; von Eggeling F; Zoll B
Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay.
American journal of medical genetics. Part A 2005;137(1):59-64.
2005: Sanjmyatav Jimsgene; Rubtsov Nikolai; Starke Heike; Schubert Joerg; Hindermann Winfried; Junker Kerstin
Identification of tumor entities of renal cell carcinoma using interphase fluorescence in situ hybridization.
The Journal of urology 2005;174(2):731-5.
2005: Vermeesch Joris Robert; Melotte Cindy; Salden Ivo; Riegel Mariluce; Trifnov Vladimir; Polityko Anna; Rumyantseva Natalia; Naumchik Irina; Starke Heike; Matthijs Gert; Schinzel Albert; Fryns Jean-Pierre; Liehr Thomas
Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype.
European journal of medical genetics 2005;48(3):319-27.
2005: Liehr Thomas; Brude Elke; Gillessen-Kaesbach Gabriele; König Rainer; Mrasek Kristin; von Eggeling Ferdinand; Starke Heike
Prader-Willi syndrome with a karyotype 47,XY,+min(15)(pter->q11.1:) and maternal UPD 15--case report plus review of similar cases.
European journal of medical genetics 2005;48(2):175-81.
2005: Mrasek Kristin; Starke Heike; Liehr Thomas
Another small supernumerary marker chromosome (sSMC) derived from chromosome 2: towards a genotype/phenotype correlation.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(3):367-70.
2005: Starke Heike; Mrasek Kristin; Liehr Thomas
Three cases with enlarged acrocentric p-arms and two cases with cryptic partial trisomies.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(3):359-60.
2005: Oliver-Bonet M; Benet J; Sun F; Navarro J; Abad C; Liehr T; Starke H; Greene C; Ko E; Martin R H
Meiotic studies in two human reciprocal translocations and their association with spermatogenic failure.
Human reproduction (Oxford, England) 2005;20(3):683-8.
2005: Liehr T; Mrasek K; Starke H; Claussen U; Schreiber G
Unusual small supernumerary marker chromosome (sSMC) 9 in a Klinefelter patient.
Cytogenetic and genome research 2005;111(2):179-81.
2005: Polityko A; Starke H; Rumyantseva N; Claussen U; Liehr T; Raskin S
Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding.
Cytogenetic and genome research 2005;111(2):171-4.
2005: Weise A; Starke H; Mrasek K; Claussen U; Liehr T
New insights into the evolution of chromosome 1.
Cytogenetic and genome research 2005;108(1-3):217-22.
2004: Liehr Thomas; Heller Anita; Eichhorn Karl-Heinz; Beensen Volkmar; Schulze Eberhart; Starke Heike; Claussen Uwe; Schreyer Isolde
Inherited cryptic chromosomal aberrations may be more easily detected in their balanced forms: a case report with hidden der(1)t(1;17)(q44;p13.2).
Prenatal diagnosis 2004;24(12):1022-4.
2004: Polityko Anna; Maltseva Olga; Rumyantseva Natalia; Khurs Olga; Seidel Jörg; Claussen Uwe; Weise Anja; Liehr Thomas; Starke Heike
Two further AHO-like syndrome patients with deletion of glypican 1 gene region in 2q37.2-q37.3.
International journal of molecular medicine 2004;14(6):977-9.
2004: Codina-Pascual M; Oliver-Bonet M; Navarro J; Starke H; Liehr T; Gutiérrez-Mateo C; Sánchez-García J F; Arango O; Egozcue J; Benet J
FISH characterization of a dicentric Yq (p11.32) isochromosome in an azoospermic male.
American journal of medical genetics. Part A 2004;127A(3):302-6.
2004: Camps Jordi; Mrasek Kristin; Prat Esther; Weise Anja; Starke Heike; Egozcue Josep; Miró Rosa; Liehr Thomas
Molecular cytogenetic characterisation of the colorectal cancer cell line SW480.
Oncology reports 2004;11(6):1215-8.
2004: Sun Fei; Oliver-Bonet Maria; Liehr Thomas; Starke Heike; Ko Evelyn; Rademaker Alfred; Navarro Joaquima; Benet Jordi; Martin Renée H
Human male recombination maps for individual chromosomes.
American journal of human genetics 2004;74(3):521-31.
2004: Liehr T; Starke H; Weise A; Lehrer H; Claussen U
Multicolor FISH probe sets and their applications.
Histology and histopathology 2004;19(1):229-37.
2004: Heller Anita; Fricke Hans-Joerg; Starke Heike; Loncarevic Ivan F; Claussen Uwe; Liehr Thomas
Characterization of a highly aberrant plasma cell leukemia karyotype: a case report.
Oncology reports 2004;11(1):89-92.
2004: Liehr T; Claussen U; Starke H
Small supernumerary marker chromosomes (sSMC) in humans.
Cytogenetic and genome research 2004;107(1-2):55-67.
2004: Lehrer H; Weise A; Michel S; Starke H; Mrasek K; Heller A; Kuechler A; Claussen U; Liehr T
The hierarchically organized splitting of chromosome bands into sub-bands analyzed by multicolor banding (MCB).
Cytogenetic and genome research 2004;105(1):25-8.
2004: Liehr T; Hickmann G; Kozlowski P; Claussen U; Starke H
Molecular-cytogenetic characterization of the origin and the presence of pericentromeric euchromatin on minute supernumerary marker chromosomes (SMCs).
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 2004;12(3):239-44.
2003: Starke Heike; Nietzel Angela; Weise Anja; Heller Anita; Mrasek Kristin; Belitz Britta; Kelbova Christine; Volleth Marianne; Albrecht Beate; Mitulla Beate; Trappe Ralf; Bartels Iris; Adolph Sabine; Dufke Andreas; Singer Sylke; Stumm Markus; Wegner Rolf-Dieter; Seidel Jörg; Schmidt Angela; Kuechler Alma; Schreyer Isolde; Claussen Uwe; von Eggeling Ferdinand; Liehr Thomas
Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification.
Human genetics 2003;114(1):51-67.
2003: Oliver-Bonet Maria; Liehr Thomas; Nietzel Angela; Heller Anita; Starke Heike; Claussen Uwe; Codina-Pascual Montserrat; Pujol Aïda; Abad Carlos; Egozcue Josep; Navarro Joaquima; Benet Jordi
Karyotyping of human synaptonemal complexes by cenM-FISH.
European journal of human genetics : EJHG 2003;11(11):879-83.
2003: Heller Anita; Trifonov Vladimir; Rubtsov Nikolai; Sauerbrey Axel; Starke Heike; Loncarevic Ivan F; Claussen Uwe; Liehr Thomas
Complex chromosomal rearrangements in a secondary acute myeloblastic leukemia after chemotherapy in TRAPS.
Oncology reports 2003;10(6):1789-92.
2003: Starke Heike; Mitulla Beate; Beensen Volkmar; Trifonov Vladimir; Rubtsov Nikolai; Heller Anita; Ziegler Monika; Neumann Annett; Claussen Uwe; Liehr Thomas
First postnatal case of mosaic del(22)/r(22).
Prenatal diagnosis 2003;23(9):765-7.
2003: Seidel Jörg; Heller Anita; Senger Gabriele; Starke Heike; Chudoba Ilse; Kelbova Christina; Tönnies Holger; Neitzel Heidemarie; Haase Claudia; Beensen Volkmar; Zintl Felix; Claussen Uwe; Liehr Thomas
A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature.
European journal of pediatrics 2003;162(9):582-8.
2003: Sauter S; von Beust G; Burfeind P; Weise A; Starke H; Liehr T; Zoll B
Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter --> p12.2)[10].
American journal of medical genetics. Part A 2003;120A(4):533-6.
2003: Liehr T; Ziegler M; Starke H; Heller A; Kuechler A; Kittner G; Beensen V; Seidel J; Hässler H; Müsebeck J; Claussen U
Conspicuous GTG-banding results of the centromere-near region can be caused by alphoid DNA heteromorphism.
Clinical genetics 2003;64(2):166-7.
2003: Mrasek Kristin; Heller Anita; Rubtsov Nikolai; Trifonov Vladimir; Starke Heike; Claussen Uwe; Liehr Thomas
Detailed Hylobates lar karyotype defined by 25-color FISH and multicolor banding.
International journal of molecular medicine 2003;12(2):139-46.
2003: Heller Anita; Rubtsov Nikolai; Kytölä Soili; Karamysheva Tatyana V; Sablina Olga V; Degtyareva Marina M; Starke Heike; Metzke Hermann; Claussen Uwe; Liehr Thomas
Highly complex karyotypic changes in acute myelogenous leukemia: a case report.
International journal of oncology 2003;23(1):139-43.
2003: Trifonov Vladimir; Seidel Jörg; Starke Heike; Martina Prechtel; Beensen Volkmar; Ziegler Monika; Hartmann Isabell; Heller Anita; Nietzel Angela; Claussen Uwe; Liehr Thomas
Enlarged chromosome 13 p-arm hiding a cryptic partial trisomy 6p22.2-pter.
Prenatal diagnosis 2003;23(5):427-30.
2003: Liehr T; Starke H; Heller A; Weise A; Beensen V; Senger G; Kittner G; Prechtel M; Claussen U; Seidel J
Evidence for a new microdeletion syndrome in 15q21.
International journal of molecular medicine 2003;11(5):575-7.
2003: Nietzel A; Albrecht B; Starke H; Heller A; Gillessen-Kaesbach G; Claussen U; Liehr T
Partial hexasomy 15pter-->15q13 including SNRPN and D15S10: first molecular cytogenetically proven case report.
Journal of medical genetics 2003;40(3):e28.
2003: Starke Heike; Mitulla Beate; Nietzel Angela; Heller Anita; Beensen Volkmar; Grosswendt Gisela; Claussen Uwe; von Eggeling Ferdinand; Liehr Thomas
First patient with trisomy 21 accompanied by an additional der(4)(:p11 --> q11:) plus partial uniparental disomy 4p15-16.
American journal of medical genetics. Part A 2003;116A(1):26-30.
2003: Weise A; Heller A; Starke H; Mrasek K; Kuechler A; Pool-Zobel B L; Claussen U; Liehr T
Multitude multicolor chromosome banding (mMCB) - a comprehensive one-step multicolor FISH banding method.
Cytogenetic and genome research 2003;103(1-2):34-9.
2003: Grasshoff U; Singer S; Liehr T; Starke H; Fode B; Schöning M; Dufke A
A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q13-->q24.1 and partial monosomy 4q27-->q28 [corrected].
Cytogenetic and genome research 2003;103(1-2):17-23.
2003: Weise A; Rittinger O; Starke H; Ziegler M; Claussen U; Liehr T
De novo 9-break-event in one chromosome 21 combined with a microdeletion in 21q22.11 in a mentally retarded boy with short stature.
Cytogenetic and genome research 2003;103(1-2):14-6.
2003: Bartels I; Schlueter G; Liehr T; von Eggeling F; Starke H; Glaubitz R; Burfeind P
Supernumerary small marker chromosome (SMC) and uniparental disomy 22 in a child with confined placental mosaicism of trisomy 22: trisomy rescue due to marker chromosome formation.
Cytogenetic and genome research 2003;101(2):103-5.
2002: Steinhaeuser Ulf; Starke Heike; Nietzel Angela; Lindenau Joerg; Ullmann Peter; Claussen Uwe; Liehr Thomas
Suspension (S)-FISH, a new technique for interphase nuclei.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2002;50(12):1697-8.
2002: Starke Heike; Seidel Jörg; Henn Wolfram; Reichardt Sylvia; Volleth Marianne; Stumm Markus; Behrend Christine; Sandig Klaus R; Kelbova Christine; Senger Gabriele; Albrecht Beate; Hansmann Ingo; Heller Anita; Claussen Uwe; Liehr Thomas
Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements.
European journal of human genetics : EJHG 2002;10(12):790-800.
2002: Liehr Thomas; Schreyer Isolde; Neumann Annett; Beensen Volkmar; Ziegler Monika; Hartmann Isabell; Starke Heike; Heller Anita; Nietzel Angela; Claussen Uwe
Two more possible pitfalls of rapid prenatal diagnostics using interphase nuclei.
Prenatal diagnosis 2002;22(6):497-9.
2002: Weise A; Starke H; Heller A; Tönnies H; Volleth M; Stumm M; Gabriele S; Nietzel A; Claussen U; Liehr T
Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes.
Journal of medical genetics 2002;39(6):434-9.
2002: Heller Anita; Starke Heike; Trifonov Vladimir; Rubtsov Nikolai; Wedding Ulrich; Loncarevic Ivan; Bleck Cordula; Claussen Uwe; Liehr Thomas
A complex translocation event between the two homologues of chromosomes 5 leading to a del(5)(q21q33) as a sole aberration in a case clinically diagnosed as CML: characterization of the aberration by multicolor banding.
International journal of oncology 2002;20(6):1179-81.
2002: Loncarevic Ivan F; Römer Jennifer; Starke Heike; Heller Anita; Bleck Cordula; Ziegler Monika; Fiedler Wolfgang; Liehr Thomas; Clement Joachim H; Claussen Uwe
Heterogenic molecular basis for loss of ABL1-BCR transcription: deletions in der(9)t(9;22) and variants of standard t(9;22) in BCR-ABL1-positive chronic myeloid leukemia.
Genes, chromosomes & cancer 2002;34(2):193-200.
2002: Liehr Thomas; Heller Anita; Starke Heike; Claussen Uwe
FISH banding methods: applications in research and diagnostics.
Expert review of molecular diagnostics 2002;2(3):217-25.
2002: Liehr Thomas; Schmidt Matthias; Starke Heike; Ziegler Monika; Kittner Gabriele; Heller Anita; Rubtsov Nikolai; Trifonov Vladimir; Claussen Uwe
First case of trisomy 13 plus mosaic trisomy 1q.
Fetal diagnosis and therapy 2002;17(3):133-6.
2002: Weise Anja; Starke Heike; Heller Anita; Uwe Claussen; Liehr Thomas
Evidence for interphase DNA decondensation transverse to the chromosome axis: a multicolor banding analysis.
International journal of molecular medicine 2002;9(4):359-61.
2002: Liehr Thomas; Heller Anita; Starke Heike; Rubtsov Nikolai; Trifonov Vladimir; Mrasek Kristin; Weise Anja; Kuechler Alma; Claussen Uwe
Microdissection based high resolution multicolor banding for all 24 human chromosomes.
International journal of molecular medicine 2002;9(4):335-9.
2002: Liehr T; Weise A; Heller A; Starke H; Mrasek K; Kuechler A; Weier H-U G; Claussen U
Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries.
Cytogenetic and genome research 2002;97(1-2):43-50.
2001: Starke H; Senger G; Kossakiewicz M; Tittelbach H; Rau D; Rubtsov N; Trifonov V; Heller A; Hartmann I; Claussen U; Liehr T
Maternal insertion of 18q11.2-q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB).
Prenatal diagnosis 2001;21(12):1049-52.
2001: Dufke A; Walczak C; Liehr T; Starke H; Trifonov V; Rubtsov N; Schöning M; Enders H; Eggermann T
Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome: extraordinary finding of an analphoid, inverted duplicated marker.
European journal of human genetics : EJHG 2001;9(8):572-6.
2001: Stankiewicz P; Thiele H; Giannakudis I; Schlicker M; Baldermann C; Krüger A; Dörr S; Starke H; Hansmann I
Kabuki syndrome-like features associated with a small ring chromosome X and XIST gene expression.
American journal of medical genetics 2001;102(3):286-92.
2001: Liehr T; Beensen V; Starke H; Hauschild R; Hempell E; Fritsche V; Hoppe C; Grosswendt G; Prechtel M; Ziegler M; Claussen U; von Eggeling F
Tetrasomy 21 due to a de novo Robertsonian translocation t(14;21) and an additional free trisomy 21.
Clinical genetics 2001;60(1):83-5.
2001: Starke H; Raida M; Trifonov V; Clement J H; Loncarevic I F; Heller A; Bleck C; Nietzel A; Rubtsov N; Claussen U; Liehr T
Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia-negative chronic myelogenous leukaemia.
British journal of haematology 2001;113(2):435-8.
2001: Liehr T; Beensen V; Hauschild R; Ziegler M; Hartmann I; Starke H; Heller A; Kähler C; Schmidt M; Reiber W; Hesse M; Claussen U
Pitfalls of rapid prenatal diagnosis using the interphase nucleus.
Prenatal diagnosis 2001;21(5):419-21.
2001: Nietzel A; Rocchi M; Starke H; Heller A; Fiedler W; Wlodarska I; Loncarevic I F; Beensen V; Claussen U; Liehr T
A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH).
Human genetics 2001;108(3):199-204.
2001: Mrasek K; Heller A; Rubtsov N; Trifonov V; Starke H; Rocchi M; Claussen U; Liehr T
Reconstruction of the female Gorilla gorilla karyotype using 25-color FISH and multicolor banding (MCB).
Cytogenetics and cell genetics 2001;93(3-4):242-8.
2000: Heller A; Seidel J; Hübler A; Starke H; Beensen V; Senger G; Rocchi M; Wirth J; Chudoba I; Claussen U; Liehr T
Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review.
Journal of medical genetics 2000;37(7):529-32.
1999: Starke H; Schreyer I; Kähler C; Fiedler W; Beensen V; Heller A; Nietzel A; Claussen U; Liehr T
Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8.
Prenatal diagnosis 1999;19(12):1169-74.
1999: Liehr T; Starke H; Beensen V; Kähler C; Harbich M; Brude E; Ziegler M; Claussen U
Translocation trisomy dup(21q) and free trisomy 21 can be distinguished by interphase-FISH.
International journal of molecular medicine 1999;3(1):11-4.

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