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	1. 10664 Accesses	Research On the origin of trisomy 21 Down syndrome Maj A Hultén, Suketu D Patel, Maira Tankimanova, Magnus Westgren, Nikos Papadogiannakis, Anna Jonsson, Erik Iwarsson Molecular Cytogenetics 2008, 1:21 (18 September 2008) Abstract \| Full text \| PDF \| PubMed \| Cited on BioMed Central
	2. 9158 Accesses	Review Human interphase chromosomes: a review of available molecular cytogenetic technologies Svetlana G Vorsanova, Yuri B Yurov, Ivan Y Iourov Molecular Cytogenetics 2010, 3:1 (11 January 2010) Abstract \| Full text \| PDF \| PubMed \| Cited on BioMed Central \| 1 comment
	3. 8175 Accesses	Research FISH mapping of Philadelphia negative BCR/ABL1 positive CML Anna Virgili, Diana Brazma, Alistair G Reid, Julie Howard-Reeves, Mikel Valgañón, Anastasios Chanalaris, Valeria AS De Melo, David Marin, Jane F Apperley, Colin Grace, Ellie P Nacheva Molecular Cytogenetics 2008, 1:14 (18 July 2008) Abstract \| Full text \| PDF \| PubMed \| Cited on BioMed Central
	4. 6660 Accesses	Case report Mosaic 22q11.2 microdeletion syndrome: diagnosis and clinical manifestations of two cases Ashutosh Halder, Manish Jain, Madhulika Kabra, Neerja Gupta Molecular Cytogenetics 2008, 1:18 (10 August 2008) Abstract \| Full text \| PDF \| PubMed \| Cited on BioMed Central
	5. 5871 Accesses	Research 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) Abstract \| Full text \| PDF \| PubMed \| Cited on BioMed Central \| 1 comment
	6. 5578 Accesses	Case report Mosaicism for r(X) and der(X)del(X)(p11.23)dup(X)(p11.21p11.22) provides insight into the possible mechanism of rearrangement Oleg A Shchelochkov, M Lance Cooper, Zhishuo Ou, Sandra Peacock, Svetlana A Yatsenko, Chester W Brown, Ping Fang, Pawel Stankiewicz, Sau Cheung Molecular Cytogenetics 2008, 1:16 (25 July 2008) Abstract \| Full text \| PDF \| PubMed \| Cited on BioMed Central
	7. 5375 Accesses	Review Fluorescence in situ hybridization in combination with the comet assay and micronucleus test in genetic toxicology Galina G Hovhannisyan Molecular Cytogenetics 2010, 3:17 (15 September 2010) Abstract \| Full text \| PDF \| PubMed
	8. 5321 Accesses	Case report A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1–q12.1 in a healthy man Laura Rodríguez, Tomas Liehr, María Martínez-Fernández, Ana Lara, Antonio Torres, María Martínez-Frías Molecular Cytogenetics 2008, 1:4 (2 April 2008) Abstract \| Full text \| PDF \| PubMed \| Cited on BioMed Central
	9. 5313 Accesses	Methodology Direct fluorescent labelling of clones by DOP PCR Liesbeth Backx, Reinhilde Thoelen, Hilde Van Esch, Joris R Vermeesch Molecular Cytogenetics 2008, 1:3 (26 March 2008) Abstract \| Full text \| PDF \| PubMed
	10. 5284 Accesses	Editorial Chromosomal mosaicism goes global Ivan Y Iourov, Svetlana G Vorsanova, Yuri B Yurov Molecular Cytogenetics 2008, 1:26 (25 November 2008) Abstract \| Full text \| PDF \| PubMed \| Cited on BioMed Central
	11. 5271 Accesses	Case report Autistic disorder associated with a paternally derived unbalanced translocation leading to duplication of chromosome 15pter-q13.2: a case report David J Wu, Nicholas J Wang, Jennette Driscoll, Naghmeh Dorrani, Dahai Liu, Marian Sigman, N Carolyn Schanen Molecular Cytogenetics 2009, 2:27 (18 December 2009) Abstract \| Full text \| PDF \| PubMed
	12. 5102 Accesses	Research Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication Blake C Ballif, Aaron Theisen, Justine Coppinger, Gordon C Gowans, Joseph H Hersh, Suneeta Madan-Khetarpal, Karen R Schmidt, Raymond Tervo, Luis F Escobar, Christopher A Friedrich, Marie McDonald, Lindsey Campbell, Jeffrey E Ming, Elaine H Zackai, Bassem A Bejjani, Lisa G Shaffer Molecular Cytogenetics 2008, 1:8 (28 April 2008) Abstract \| Full text \| PDF \| PubMed \| Cited on BioMed Central
	13. 5022 Accesses	Research 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) Abstract \| Full text \| PDF \| PubMed
	14. 4820 Accesses	Editorial A new open access journal for a rapidly evolving biomedical field: introducing Molecular Cytogenetics Yuri B Yurov, Thomas Liehr, Lisa G Shaffer, Ivan Y Iourov, Svetlana G Vorsanova Molecular Cytogenetics 2008, 1:1 (26 March 2008) Abstract \| Full text \| PDF \| PubMed
	15. 4761 Accesses	Review Cytogenetic contribution to uniparental disomy (UPD) Thomas Liehr Molecular Cytogenetics 2010, 3:8 (29 March 2010) Abstract \| Full text \| PDF \| PubMed
	16. 4726 Accesses	Research 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) Abstract \| Full text \| PDF \| PubMed
	17. 4704 Accesses	Research 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) Abstract \| Full text \| PDF \| PubMed
	18. 4651 Accesses	Case report Application of molecular cytogenetic techniques to clarify apparently balanced complex chromosomal rearrangements in two patients with an abnormal phenotype: case report Paula JP de Vree, Marleen EH Simon, Marieke F van Dooren, Gerda HT Stoevelaar, José TW Hilkmann, Michel A Rongen, Gido CM Huijbregts, Annemieke JMH Verkerk, Pino J Poddighe Molecular Cytogenetics 2009, 2:15 (13 July 2009) Abstract \| Full text \| PDF \| PubMed \| Cited on BioMed Central
	19. 4579 Accesses	Research 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, Héctor N Seuánez Molecular Cytogenetics 2009, 2:20 (7 October 2009) Abstract \| Full text \| PDF \| PubMed
	20. 4520 Accesses	Research Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH Christine Tyson, Ying Qiao, Chansonette Harvard, Xudong Liu, Francois P Bernier, Barbara McGillivray, Sandra A Farrell, Laura Arbour, Albert E Chudley, Lorne Clarke, William Gibson, Sarah Dyack, Ross McLeod, Teresa Costa, Margot I VanAllen, Siu-li Yong, Gail E Graham, Patrick MacLeod, Millan S Patel, Jane Hurlburt, Jeanette JA Holden, Suzanne ME Lewis, Evica Rajcan-Separovic Molecular Cytogenetics 2008, 1:23 (11 November 2008) Abstract \| Full text \| PDF \| PubMed \| Cited on BioMed Central
	21. 4395 Accesses	Review Comparison of mitotic cell death by chromosome fragmentation to premature chromosome condensation Joshua B Stevens, Batoul Y Abdallah, Sarah M Regan, Guo Liu, Steven W Bremer, Christine J Ye, Henry H Heng Molecular Cytogenetics 2010, 3:20 (19 October 2010) Abstract \| Full text \| PDF \| PubMed
	22. 4376 Accesses	Research Evidence-based genomic diagnosis characterized chromosomal and cryptic imbalances in 30 elderly patients with myelodysplastic syndrome and acute myeloid leukemia Renu Bajaj, Fang Xu, Bixia Xiang, Katherine Wilcox, Autumn J DiAdamo, Rachana Kumar, Alexandra Pietraszkiewicz, Stephanie Halene, Peining Li Molecular Cytogenetics 2011, 4:3 (20 January 2011) Abstract \| Full text \| PDF \| PubMed
	23. 4349 Accesses	Research Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations Paola Evangelidou, Carolina Sismani, Marios Ioannides, Christodoulos Christodoulou, George Koumbaris, Ioannis Kallikas, Ioannis Georgiou, Voula Velissariou, Philippos C Patsalis Molecular Cytogenetics 2010, 3:24 (26 November 2010) Abstract \| Full text \| PDF \| PubMed
	24. 4307 Accesses	Research 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) Abstract \| Full text \| PDF \| PubMed
	25. 4211 Accesses	Research On the paternal origin of trisomy 21 Down syndrome Maj A Hultén, Suketu D Patel, Magnus Westgren, Nikos Papadogiannakis, Anna Jonsson, Jon Jonasson, Erik Iwarsson Molecular Cytogenetics 2010, 3:4 (23 February 2010) Abstract \| Full text \| PDF \| PubMed