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Kristin Mrasek

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Thomas Liehr; Kristin Mrasek; Moneeb Ak Othman; Anja Weise; Nadine Aust; Xiaobo Fan; Ahmed B Hamid; Elisabeth Klein; Nadezda Kosyakova
Multicolor FISH methods in current clinical diagnostics.
Thomas Liehr; Kristin Mrasek; C Venner; Anja Weise; N Aust; R S Guilherme; E Klein; Nadezda Kosyakova; A B Hamid
Clinical impact of somatic mosaicism in cases with small supernumerary marker chromosomes.
Nestor L Lopez Corrales; Thomas Liehr; Kristin Mrasek; Martin Voigt; Nadezda Kosyakova
Copy number variations (CNVs) in human pluripotent cell-derived neuroprogenitors.

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2013: Thomas Liehr; Kristin Mrasek; Moneeb Ak Othman; Anja Weise; Nadine Aust; Xiaobo Fan; Ahmed B Hamid; Elisabeth Klein; Nadezda Kosyakova
Multicolor FISH methods in current clinical diagnostics.
Expert review of molecular diagnostics 2013;13(3):251-5.
2013: Thomas Liehr; Kristin Mrasek; C Venner; Anja Weise; N Aust; R S Guilherme; E Klein; Nadezda Kosyakova; A B Hamid
Clinical impact of somatic mosaicism in cases with small supernumerary marker chromosomes.
Cytogenetic and genome research 2013;139(3):158-63.
2012: Nestor L Lopez Corrales; Thomas Liehr; Kristin Mrasek; Martin Voigt; Nadezda Kosyakova
Copy number variations (CNVs) in human pluripotent cell-derived neuroprogenitors.
Gene 2012;506(2):377-9.
2012: Ahmed B Hamid; David Hardekopf; Tatyana Karamysheva; Roberta Santos Guilherme; Nadezda Kosayakova; Katharina Kreskowski; Thomas Liehr; Kristin Mrasek; Sona Pekova; Martin Voigt; Rebecca Wagner; Anja Weise; Elisabeth Klein
How to narrow down chromosomal breakpoints in small and large derivative chromosomes--a new probe set.
Journal of applied genetics 2012;53(3):259-69.
2012: Anja Weise; samarth Bhatt; David Hardekopf; Elisabeth Klein; Nadezda Kosyakova; Juan C Llerena; Kristin Mrasek; Milene Mulatinho; Sona Pekova; Thomas Liehr
Microdeletion and microduplication syndromes.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2012;60(5):346-58.
2012: Ke Ma; Kristin Mrasek; Li Qiu; Luciana Gonçalves Quintana; Jun Zhang; Thomas Liehr; Zheng Li
Common fragile sites: genomic hotspots of DNA damage and carcinogenesis.
International journal of molecular sciences 2012;13(9):11974-99.
2012: Milene Vianna Mulatinho; Sona Pekova; Nagesh Rao; Fernanda Scalco; Anja Weise; Cassio Luiz de Carvalho Serao; David Hardekopf; Thomas Liehr; Kristin Mrasek; Juan Clinton Llerena
Severe intellectual disability, omphalocele, hypospadia and high blood pressure associated to a deletion at 2q22.1q22.3: case report.
Molecular cytogenetics 2012;5(1):30.
2011: Claudia Backsch; Andreas Clad; Mieczyslaw Gajda; Thomas Liehr; Melanie Liesenfeld; Kristin Mrasek; Birgit Pauly; Ingo B Runnebaum; Cornelia Scheungraber; Evelin Schrock; Matthias Dürst
Two novel unbalanced whole arm translocations are frequently detected in cervical squamous cell carcinoma.
Cancer genetics 2011;204(12):646-53.
2011: Thomas Liehr; I Bartels; B Zoll; E Ewers; Kristin Mrasek; Nadezda Kosyakova; M Merkas; A B Hamid; Ferdinand von Eggeling; N Posorski; Anja Weise
Is there a yet unreported unbalanced chromosomal abnormality without phenotypic consequences in proximal 4p?
Cytogenetic and genome research 2011;132(1-2):121-3.
2010: M Santos; Kristin Mrasek; I Madrigal; M R Martorell; A González-Meneses; G Rodríguez-Criado; M Milà; Thomas Liehr; C Fuster
Characterization of a complex cryptic mosaicism for an sSMC derived from the X chromosome present in a boy with congenital malformations.
American journal of medical genetics. Part A 2010;152A(10):2661-3.
2010: Thomas Liehr; Tatyana Karamysheva; Martina Merkas; Lukrecija Brecevic; Ahmed B Hamid; Elisabeth Ewers; Kristin Mrasek; Nadezda Kosyakova; Anja Weise
Somatic mosaicism in cases with small supernumerary marker chromosomes.
Current genomics 2010;11(6):432-9.
2010: Hasmik Mkrtchyan; Madeleine Gross; Sophie Hinreiner; Anna Polytiko; Marina Manvelyan; Kristin Mrasek; Nadezda Kosyakova; Elisabeth Ewers; Heike Nelle; Thomas Liehr; samarth Bhatt; Karen Thoma; Erich Gebhart; Sylvia Wilhelm; Raimund Fahsold; Marianne Volleth; Anja Weise
The human genome puzzle - the role of copy number variation in somatic mosaicism.
Current genomics 2010;11(6):426-31.
2010: Heike Nelle; Isolde Schreyer; Elisabeth Ewers; Kristin Mrasek; Nadezda Kosyakova; Martina Merkas; Ahmed Basheer Hamid; Raimund Fahsold; Anikó Ujfalusi; Jasen Anderson; Nikolai Rubtsov; Alma Küchler; Ferdinand von Eggeling; Julia Hentschel; Anja Weise; Thomas Liehr
Presence of harmless small supernumerary marker chromosomes hampers molecular genetic diagnosis: a case report.
Molecular medicine reports 2010;3(4):571-4.
2010: Kristin Mrasek; Christiane Schoder; Anne-Christin Teichmann; Katja Behr; Britta Franze; Kathleen Wilhelm; Nancy Blaurock; Uwe Claussen; Thomas Liehr; Anja Weise
Global screening and extended nomenclature for 230 aphidicolin-inducible fragile sites, including 61 yet unreported ones.
International journal of oncology 2010;36(4):929-40.
2010: Christiane Schoder; Thomas Liehr; Eunike Velleuer; Kathleen Wilhelm; Nancy Blaurock; Anja Weise; Kristin Mrasek
New aspects on chromosomal instability: chromosomal break-points in Fanconi anemia patients co-localize on the molecular level with fragile sites.
International journal of oncology 2010;36(2):307-12.
2010: Thomas Liehr; Anja Weise; Sophie Hinreiner; Hasmik Mkrtchyan; Kristin Mrasek; Nadezda Kosyakova
Characterization of chromosomal rearrangements using multicolor-banding (MCB/m-band).
Methods in molecular biology (Clifton, N.J.) 2010;659():231-8.
2010: Dilek Aktas; Eda G Utine; Kristin Mrasek; Anja Weise; Ferdinand von Eggeling; Kalbiye Yalaz; Nicole Posorski; Nurten Akarsu; Mehmet Alikasifoglu; Thomas Liehr; Ergul Tuncbilek
Derivative chromosome 1 and GLUT1 deficiency syndrome in a sibling pair.
Molecular cytogenetics 2010;3(1):10.
2010: Hasmik Mkrtchyan; Madeleine Gross; Sophie Hinreiner; Anna Polytiko; Marina Manvelyan; Kristin Mrasek; Nadezda Kosyakova; Elisabeth Ewers; Heike Nelle; Thomas Liehr; Marianne Volleth; Anja Weise
Early embryonic chromosome instability results in stable mosaic pattern in human tissues.
PloS one 2010;5(3):e9591.
2009: Marina Manvelyan; Philipp Kempf; Anja Weise; Kristin Mrasek; Anita Heller; Amelie Lier; Klaus Höffken; Hans-Jörg Fricke; Herbert G Sayer; Thomas Liehr; Hasmik Mkrtchyan
Preferred co-localization of chromosome 8 and 21 in myeloid bone marrow cells detected by three dimensional molecular cytogenetics.
International journal of molecular medicine 2009;24(3):335-41.
2009: Emmanouil Manolakos; Annalisa Vetro; Stylianos Kitmirides; Ioannis Papoulidis; Nadezda Kosyakova; Kristin Mrasek; Anja Weise; Emmanouil Agapitos; Sandro Orru; Panagiotis Peitsidis; Thomas Liehr; Michael B Petersen
Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGH.
Prenatal diagnosis 2009;29(9):884-8.
2009: L Uroz; Thomas Liehr; Kristin Mrasek; Cristina Templado
Centromere-specific multicolour fluorescence in situ hybridization on human spermatocyte I and II metaphases.
Human reproduction (Oxford, England) 2009;24(8):2029-33.
2009: Anja Weise; Elisabeth Ewers; Nadezda Kosyakova; Hasmik Mkrtchyan; Kristin Mrasek; Thomas Liehr
Diagnostic applications of fluorescence in situ hybridization.
Expert opinion on medical diagnostics 2009;3(4):453-60.
2009: Emel Ergul; Thomas Liehr; Kristin Mrasek; Ali Sazci
A de novo complex chromosome rearrangement involving three chromosomes (2, 13, and 18) in an oligospermic male.
Fertility and sterility 2009;92(1):391.e9-391.e12.
2009: Dilek Aktas; Anja Weise; Eda Utine; Dursun Alehan; Kristin Mrasek; Ferdinand von Eggeling; Heike Thieme; Ergul Tuncbilek; Thomas Liehr
Clinically abnormal case with paternally derived partial trisomy 8p23.3 to 8p12 including maternal isodisomy of 8p23.3: a case report.
Molecular cytogenetics 2009;2():14.
2009: Thomas Liehr; Markus Stumm; Rolf-Dieter Wegner; S Bhatt; P Hickmann; P C Patsalis; M Meins; S Morlot; V Klaschka; E Ewers; S Hinreiner; Kristin Mrasek; Nadezda Kosyakova; W W Cai; Sau Wai Cheung; Anja Weise
10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences.
Cytogenetic and genome research 2009;124(1):102-5.
2009: Nadezda Kosyakova; Anja Weise; Kristin Mrasek; Uwe Claussen; Thomas Liehr; Heike Nelle
The hierarchically organized splitting of chromosomal bands for all human chromosomes.
Molecular cytogenetics 2009;2():4.
2008: Marina Manvelyan; Mariluce Riegel; Monica Santos; Carme Fuster; Franck Pellestor; Marie-Luise Mazaurik; Bernt Schulze; Anna Polityko; Hanne Tittelbach; Gisela Reising-Ackermann; Britta Belitz; Ute Hehr; Christine Kelbova; Marianne Volleth; Elisabeth Gödde; Jasen Anderson; Peter Küpferling; Sigrid Köhler; Hans-Christoph Duba; Andreas Dufke; Dilek Aktas; Thomas Martin; Isolde Schreyer; Elisabeth Ewers; Daniela Reich; Kristin Mrasek; Anja Weise; Thomas Liehr
Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literature.
International journal of molecular medicine 2008;21(6):705-14.
2008: Anja Weise; Kristin Mrasek; Ina Fickelscher; Uwe Claussen; Sau Wai Cheung; Wei Wen Cai; Thomas Liehr; Nadezda Kosyakova
Molecular definition of high-resolution multicolor banding probes: first within the human DNA sequence anchored FISH banding probe set.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2008;56(5):487-93.
2008: Anja Weise; Madeleine Gross; Kristin Mrasek; Hasmik Mkrtchyan; B Horsthemke; C Jonsrud; Ferdinand von Eggeling; S Hinreiner; V Witthuhn; Uwe Claussen; Thomas Liehr
Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell level.
International journal of molecular medicine 2008;21(2):189-200.
2008: Marina Manvelyan; Friederike Hunstig; samarth Bhatt; Kristin Mrasek; Franck Pellestor; Anja Weise; Isabella Simonyan; Rouben Aroutiounian; Thomas Liehr
Chromosome distribution in human sperm - a 3D multicolor banding-study.
Molecular cytogenetics 2008;1():25.
2008: Kristin Mrasek; G Krüger; I Bauer; J Müller-Navia; Thomas Liehr; Anja Weise
A new unbalanced chromosomal abnormality in 1q31.1 to 1q32 without phenotypic consequences.
Cytogenetic and genome research 2008;121(3-4):286-7.
2008: Nilüfer Karadeniz; Kristin Mrasek; Anja Weise
Further delineation of complex chromosomal rearrangements in fertile male using multicolor banding.
Molecular cytogenetics 2008;1():17.
2008: Thomas Liehr; Kristin Mrasek; Nadezda Kosyakova; Caroline Mackie Ogilvie; Joris R Vermeesch; Vladimir Trifonov; Nikolai Rubtsov
Small supernumerary marker chromosomes (sSMC) in humans; are there B chromosomes hidden among them.
Molecular cytogenetics 2008;1():12.
2008: Marina Manvelyan; Friederike Hunstig; Kristin Mrasek; samarth Bhatt; Franck Pellestor; Anja Weise; Thomas Liehr
Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon.
Molecular cytogenetics 2008;1():9.
2007: Mònica Santos; Kristin Mrasek; Maria Angels Rigola; Heike Starke; Thomas Liehr; Carme Fuster
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: G Eda Utine; D Aktas; Yasemin Alanay; S Gücer; Ergul Tuncbilek; Kristin Mrasek; Thomas Liehr
Distal partial trisomy 1q: report of two cases and a review of the literature.
Prenatal diagnosis 2007;27(9):865-71.
2007: M Manvelyan; Isolde Schreyer; I Höls-Herpertz; S Köhler; R Niemann; U Hehr; Britta Belitz; Iris Bartels; J Götz; D Huhle; M Kossakiewicz; H Tittelbach; S Neubauer; Anna Polityko; M-L Mazauric; Rolf-Dieter Wegner; Markus Stumm; P Küpferling; F Süss; H Kunze; Anja Weise; Thomas Liehr; Kristin Mrasek
Forty-eight new cases with infertility due to balanced chromosomal rearrangements: detailed molecular cytogenetic analysis of the 90 involved breakpoints.
International journal of molecular medicine 2007;19(6):855-64.
2007: Holger Tönnies; Joanna Pietrzak; Ewa Bocian; Kay MacDermont; Alma Kuechler; Britta Belitz; Udo Trautmann; Angela Schmidt; Berndt Schulze; Laura Rodríguez; Franz Binkert; Catharine Yardin; Nadezda Kosyakova; Marianne Volleth; Hasmik Mkrtchyan; Isolde Schreyer; Ferdinand von Eggeling; Anja Weise; Kristin Mrasek; Thomas Liehr
New immortalized cell lines of patients with small supernumerary marker chromosome: towards the establishment of a cell bank.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2007;55(6):651-60.
2007: Sevim Balci; Aysun Unal; Ozlem Engiz; Dilek Aktas; Thomas Liehr; Madelaine Gross; Kristin Mrasek; Serap Saygi
Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X;19) (q11.1-11.2;p13.3).
Developmental medicine and child neurology 2007;49(3):219-24.
2007: Thomas Liehr; Kristin Mrasek; S Hinreiner; D Reich; E Ewers; I Bartels; J Seidel; N Emmanuil; M Petesen; A Polityko; A Dufke; I Iourov; V Trifonov; J Vermeesch; Anja Weise
Small supernumerary marker chromosomes (sSMC) in patients with a 45,X/46,X,+mar karyotype - 17 new cases and a review of the literature.
Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation 2007;1(6):353-62.
2007: Thomas Liehr; G Eda Utine; Udo Trautmann; A Rauch; Alma Kuechler; Joanna Pietrzak; J Pietracz; Ewa Bocian; Nadezda Kosyakova; Kristin Mrasek; Koray Boduroglu; Anja Weise; Dilek Aktas
Neocentric small supernumerary marker chromosomes (sSMC)--three more cases and review of the literature.
Cytogenetic and genome research 2007;118(1):31-7.
2007: Joanna Pietrzak; Kristin Mrasek; Ewa Obersztyn; Pawel Stankiewicz; Nadezda Kosyakova; Anja Weise; Sau Wai Cheung; Wei-Wen Cai; Ferdinand von Eggeling; Tadeusz Mazurczak; Ewa Bocian; Thomas Liehr
Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patients.
Journal of applied genetics 2007;48(2):167-75.
2006: Eleftheria Papadopoulou; Stavros Sifakis; Catherine Sarri; Jolanda Gyftodimou; Thomas Liehr; Kristin Mrasek; Maria Kalmanti; Michael B Petersen
A report of pure 7p duplication syndrome and review of the literature.
American journal of medical genetics. Part A 2006;140(24):2802-6.
2006: Sevim Balci; Ozlem Engiz; Dilek Aktaş; Ibrahim Vargel; M Sinan Beksaç; Kristin Mrasek; Joris R Vermeesch; Thomas Liehr
Ring chromosome 4 and Wolf-Hirschhorn syndrome (WHS) in a child with multiple anomalies.
American journal of medical genetics. Part A 2006;140(6):628-32.
2006: Constanze Karst; Vladimir Trifonov; Svetlana A. Romanenko; Uwe Claussen; Kristin Mrasek; Susanne Michel; Philip Avner; Thomas Liehr
Molecular cytogenetic characterization of the mouse cell line WMP2 by spectral karyotyping and multicolor banding applying murine probes.
International journal of molecular medicine 2006;17(2):209-13.
2006: Andreas Dufke; S Singer; S Borell-Kost; M Stotter; D A Pflumm; Ulrike Angelika Mau-Holzmann; Heike Starke; Kristin Mrasek; Herbert Enders
De novostructural chromosomal imbalances: molecular cytogenetic characterization of partial trisomies.
Cytogenetic and genome research 2006;114(3-4):342-50.
2006: Catherine Sarri; Yolanda Gyftodimou; Maria Grigoriadou; Effie Pandelia; S Kalogirou; Haris Kokotas; Kristin Mrasek; Anja Weise; Michael B Petersen
Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual face.
Cytogenetic and genome research 2006;114(3-4):330-7.
2006: Lukrecija Brecevic; S Michel; Heike Starke; K Müller; Nadezda Kosyakova; Kristin Mrasek; Anja Weise; Thomas Liehr
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: Thomas Liehr; Heike Starke; Anita Heller; Nadezda Kosyakova; Kristin Mrasek; Madeleine Gross; Constanze Karst; U Steinhaeuser; F Hunstig; Ina Fickelscher; Alma Kuechler; Vladimir Trifonov; Svetlana A. Romanenko; Anja Weise
Multicolor fluorescence in situ hybridization (FISH) applied to FISH-banding.
Cytogenetic and genome research 2006;114(3-4):240-4.
2006: Thomas Liehr; Madeleine Gross; Constanze Karst; Melanie Glaser; Kristin Mrasek; Heike Starke; Anja Weise; Hasmik Mkrtchyan; Alma Kuechler
FISH banding in tumor cytogenetics.
Cancer genetics and cytogenetics 2006;164(1):88-9.
2006: Thomas Liehr; Kristin Mrasek; Anja Weise; Andreas Dufke; L Rodríguez; N Martínez Guardia; A Sanchís; Joris R Vermeesch; C Ramel; Anna Polityko; O A Haas; J Anderson; Uwe Claussen; Ferdinand von Eggeling; Heike Starke
Small supernumerary marker chromosomes--progress towards a genotype-phenotype correlation.
Cytogenetic and genome research 2006;112(1-2):23-34.
2005: Vladimir Trifonov; Constanze Karst; Uwe Claussen; Kristin Mrasek; Susanne Michel; Philip Avner; Thomas Liehr
Microdissection-derived murine mcb probes from somatic cell hybrids.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(6):791-2.
2005: Thomas Liehr; Elke Brude; Gabriele Gillessen-Kaesbach; Rainer König; Kristin Mrasek; Ferdinand von Eggeling; Heike Starke
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: Kristin Mrasek; Heike Starke; Thomas Liehr
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: Heike Starke; Kristin Mrasek; Thomas Liehr
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: Thomas Liehr; Kristin Mrasek; Heike Starke; Uwe Claussen; G Schreiber
Unusual small supernumerary marker chromosome (sSMC) 9 in a Klinefelter patient.
Cytogenetic and genome research 2005;111(2):179-81.
2005: Anja Weise; Heike Starke; Kristin Mrasek; Uwe Claussen; Thomas Liehr
New insights into the evolution of chromosome 1.
Cytogenetic and genome research 2005;108(1-3):217-22.
2004: Jordi Camps; Kristin Mrasek; Esther Prat; Anja Weise; Heike Starke; Josep Egozcue; Rosa Miró; Thomas Liehr
Molecular cytogenetic characterisation of the colorectal cancer cell line SW480.
Oncology reports 2004;11(6):1215-8.
2004: H Lehrer; Anja Weise; Susanne Michel; Heike Starke; Kristin Mrasek; Anita Heller; Alma Kuechler; Uwe Claussen; Thomas Liehr
The hierarchically organized splitting of chromosome bands into sub-bands analyzed by multicolor banding (MCB).
Cytogenetic and genome research 2004;105(1):25-8.
2003: Heike Starke; Angela Nietzel; Anja Weise; Anita Heller; Kristin Mrasek; Britta Belitz; Christine Kelbova; Marianne Volleth; Beate Albrecht; Beate Mitulla; Ralf Trappe; Iris Bartels; Sabine Adolph; Andreas Dufke; Sylke Singer; Markus Stumm; Rolf-Dieter Wegner; Jörg Seidel; Angela Schmidt; Alma Kuechler; Isolde Schreyer; Uwe Claussen; Ferdinand von Eggeling; Thomas Liehr
Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification.
Human genetics 2003;114(1):51-67.
2003: Kristin Mrasek; Anita Heller; Nikolai Rubtsov; Vladimir Trifonov; Heike Starke; Uwe Claussen; Thomas Liehr
Detailed Hylobates lar karyotype defined by 25-color FISH and multicolor banding.
International journal of molecular medicine 2003;12(2):139-46.
2003: Anja Weise; Anita Heller; Heike Starke; Kristin Mrasek; Alma Kuechler; Beatrice L Pool-Zobel; Uwe Claussen; Thomas Liehr
Multitude multicolor chromosome banding (mMCB) - a comprehensive one-step multicolor FISH banding method.
Cytogenetic and genome research 2003;103(1-2):34-9.
2002: Thomas Liehr; Anita Heller; Heike Starke; Nikolai Rubtsov; Vladimir Trifonov; Kristin Mrasek; Anja Weise; Alma Kuechler; Uwe Claussen
Microdissection based high resolution multicolor banding for all 24 human chromosomes.
International journal of molecular medicine 2002;9(4):335-9.
2002: Thomas Liehr; Anja Weise; Anita Heller; Heike Starke; Kristin Mrasek; Alma Kuechler; Heinz-Ulrich G Weier; Uwe Claussen
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: Kristin Mrasek; Anita Heller; Nikolai Rubtsov; Vladimir Trifonov; Heike Starke; M Rocchi; Uwe Claussen; Thomas Liehr
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.