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Genomic amplification of BCR/ABL1 and a region downstream of ABL1 in chronic myeloid leukaemia: a FISH mapping study of CML patients and cell lines
Anna Virgili, Elisabeth P Nacheva
Molecular Cytogenetics 2010, 3:15 (1 September 2010)
[Abstract] [Provisional PDF]
Research
X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation
Susana I Ferreira, Eunice Matoso, Marta Pinto, Joana Almeida, Thomas Liehr, Joana B Melo, Isabel M Carreira
Molecular Cytogenetics 2010, 3:14 (20 July 2010)
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Comparative analysis of copy number detection by whole-genome BAC and oligonucleotide array CGH
Nicholas J Neill, Beth S Torchia, Bassem A Bejjani, Lisa G Shaffer, Blake C Ballif
Molecular Cytogenetics 2010, 3:11 (29 June 2010)
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Derivative chromosome 1 and GLUT1 deficiency syndrome in a sibling pair
Dilek Aktas, Eda G Utine, Kristin Mrasek, Anja Weise, Ferdinand von Eggeling, Kalbiye Yalaz, Nicole Posorski, Nurten Akarsu, Mehmet Alikasifoglu, Thomas Liehr, Ergul Tuncbilek
Molecular Cytogenetics 2010, 3:10 (28 May 2010)
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Validation and implementation of array comparative genomic hybridisation as a first line test in place of postnatal karyotyping for genome imbalance
Joo Wook Ahn, Kathy Mann, Sally Walsh, Marwa Shehab, Sarah Hoang, Zoe Docherty, Shehla Mohammed, Caroline Mackie Ogilvie
Molecular Cytogenetics 2010, 3:9 (15 April 2010)
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Two siblings with immunodeficiency, facial abnormalities and chromosomal instability without mutation in DNMT3B gene but liability towards malignancy; a new chromatin disorder delineation?
Anna Polityko, Olga Khurs, Natalia Rumyantseva, Irina Naumchik, Nadezda Kosyakova, Holger Tönnies, Karl Sperling, Heidemarie Neitzel, Anja Weise, Thomas Liehr
Molecular Cytogenetics 2010, 3:5 (8 March 2010)
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On the paternal origin of trisomy 21 Down syndrome
Maj A Hultén, Suketu D Patel, Magnus Westgren, Nikos Papadogiannakis, Anna Maria Jonsson, Jon Jonasson, Erik Iwarsson
Molecular Cytogenetics 2010, 3:4 (23 February 2010)
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8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families
John CK Barber, Dave Bunyan, Merryl Curtis, Denise Robinson, Susanne Morlot, Anette Dermitzel, Thomas Liehr, Claudia Alves, Joana Trindade, Ana I Paramos, Clare Cooper, Kevin Ocraft, Emma-Jane Taylor, Viv K Maloney
Molecular Cytogenetics 2010, 3:3 (18 February 2010)
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Detailed analysis of X chromosome inactivation in a 49,XXXXX pentasomy
Lucia M Moraes, Leila CA Cardoso, Vera LS Moura, Miguel AM Moreira, Albert N Menezes, Juan C Llerena Jr, Héctor N Seuánez
Molecular Cytogenetics 2009, 2:20 (7 October 2009)
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Chromosome territories, X;Y translocation and Premature Ovarian Failure: is there a relationship?
Sara Lissoni, Simona Baronchelli, Nicoletta Villa, Valeria Lucchini, Enrico Betri, Pietro Cavalli, Leda Dalprà
Molecular Cytogenetics 2009, 2:19 (27 September 2009)
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Candidate metastasis suppressor genes uncovered by array comparative genomic hybridization in a mouse allograft model of prostate cancer
Yajun Yi, Srinivas Nandana, Thomas Case, Colleen Nelson, Tatjana Radmilovic, Robert J Matusik, Karen D Tsuchiya
Molecular Cytogenetics 2009, 2:18 (26 September 2009)
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Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31  qter) detected in an autistic boy
Isabel M Carreira, Joana B Melo, Carlos Rodrigues, Liesbeth Backx, Joris Vermeesch, Anja Weise, Nadezda Kosyakova, Guiomar Oliveira, Eunice Matoso
Molecular Cytogenetics 2009, 2:16 (4 August 2009)
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Automated detection of residual cells after sex-mismatched stem-cell transplantation  evidence for presence of disease-marker negative residual cells
Jörn Erlecke, Isabell Hartmann, Martin Hoffmann, Torsten Kroll, Heike Starke, Anita Heller, Alexander Gloria, Herbert G Sayer, Tilman Johannes, Uwe Claussen, Thomas Liehr, Ivan F Loncarevic
Molecular Cytogenetics 2009, 2:12 (29 May 2009)
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Microdeletion syndromes disclose replication timing alterations of genes unrelated to the missing DNA
Josepha Yeshaya, Itay Amir, Ayelet Rimon, Jane Freedman, Mordechai Shohat, Lydia Avivi
Molecular Cytogenetics 2009, 2:11 (14 March 2009)
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Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation
Bernd Auber, Verena Bruemmer, Barbara Zoll, Peter Burfeind, Detlef Boehm, Thomas Liehr, Knut Brockmann, Ekkehard Wilichowski, Loukas Argyriou, Iris Bartels
Molecular Cytogenetics 2009, 2:10 (12 March 2009)
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MODY-like diabetes associated with an apparently balanced translocation: possible involvement of MPP7 gene and cell polarity in the pathogenesis of diabetes
Elizabeth J Bhoj, Stefano Romeo, Marco G Baroni, Guy Bartov, Roger A Schultz, Andrew R Zinn
Molecular Cytogenetics 2009, 2:5 (13 February 2009)
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The hierarchically organized splitting of chromosomal bands for all human chromosomes
Nadezda Kosyakova, Anja Weise, Kristin Mrasek, Uwe Claussen, Thomas Liehr, Heike Nelle
Molecular Cytogenetics 2009, 2:4 (26 January 2009)
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Validation of DNA probes for molecular cytogenetics by mapping onto immobilized circular DNA
Karin M Greulich-Bode, Mei Wang, Andreas P Rhein, Jingly F Weier, Heinz-Ulli G Weier
Molecular Cytogenetics 2008, 1:28 (23 December 2008)
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De novo complex intra chromosomal rearrangement after ICSI: characterisation by BACs micro array-CGH
Serdar Kasakyan, Laurence Lohmann, Azeddine Aboura, Mazin Quimsiyeh, Yves Menezo, Gerard Tachdjian, Moncef Benkhalifa
Molecular Cytogenetics 2008, 1:27 (23 December 2008)
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Chromosome distribution in human sperm a 3D multicolor banding-study
Marina Manvelyan, Friederike Hunstig, Samarth Bhatt, Kristin Mrasek, Franck Pellestor, Anja Weise, Isabella Simonyan, Rouben Aroutiounian, Thomas Liehr
Molecular Cytogenetics 2008, 1:25 (14 November 2008)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles] [Cited on BioMed Central]
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