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	1. 4602 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
	2. 3529 Accesses	Review The genome diversity and karyotype evolution of mammals Alexander S Graphodatsky, Vladimir A Trifonov, Roscoe Stanyon Molecular Cytogenetics 2011, 4:22 (12 October 2011) Abstract \| Full text \| PDF \| PubMed
	3. 3504 Accesses	Research Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases Sang-Jin Park, Eun Jung, Ran-Suk Ryu, Hyun Kang, Jung-Min Ko, Hyon J Kim, Chong Cheon, Sang-Hyun Hwang, Ho-Young Kang Molecular Cytogenetics 2011, 4:12 (9 May 2011) Abstract \| Full text \| PDF \| PubMed
	4. 3046 Accesses	Methodology Selection of single blastocysts for fresh transfer via standard morphology assessment alone and with array CGH for good prognosis IVF patients: results from a randomized pilot study Zhihong Yang, Jiaen Liu, Gary S Collins, Shala A Salem, Xiaohong Liu, Sarah S Lyle, Alison C Peck, E Scott Sills, Rifaat D Salem Molecular Cytogenetics 2012, 5:24 (2 May 2012) Abstract \| Provisional PDF \| PubMed \| Editor’s summary Selectively implanting euploid embryos, with a normal number of chromosomes, significantly increases pregnancy rates for IVF patients, highlighting the importance of offering preimplantation genetic screening.
	5. 2923 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
	6. 2778 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
	7. 2749 Accesses	Hypothesis On the origin of crossover interference: A chromosome oscillatory movement (COM) model Maj A Hultén Molecular Cytogenetics 2011, 4:10 (8 April 2011) Abstract \| Full text \| PDF \| PubMed
	8. 2626 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
	9. 2575 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
	10. 2567 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
	11. 2443 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
	12. 2383 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
	13. 2284 Accesses	Research Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells Roberto Valli, Cristina Marletta, Barbara Pressato, Giuseppe Montalbano, Francesco Lo Curto, Francesco Pasquali, Emanuela Maserati Molecular Cytogenetics 2011, 4:13 (9 May 2011) Abstract \| Full text \| PDF \| PubMed
	14. 2254 Accesses	Case report Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy Emmanouil Manolakos, Catherine Sarri, Annalisa Vetro, Konstantinos Kefalas, Eleni Leze, Christalena Sofocleus, George Kitsos, Konstantina Merou, Haris Kokotas, Anna Papadopoulou, Achilleas Attilakos, Michael B Petersen, Sofia Kitsiou-Tzeli Molecular Cytogenetics 2011, 4:6 (23 February 2011) Abstract \| Full text \| PDF \| PubMed \| 1 comment
	15. 2177 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
	16. 2059 Accesses	Review Cytogenetic contribution to uniparental disomy (UPD) Thomas Liehr Molecular Cytogenetics 2010, 3:8 (29 March 2010) Abstract \| Full text \| PDF \| PubMed
	17. 1921 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
	18. 1890 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
	19. 1853 Accesses	Case report Chromosome 12q24.31-q24.33 deletion causes multiple dysmorphic features and developmental delay: First mosaic patient and overview of the phenotype related to 12q24qter defects Jawaher Al-Zahrani, Naji Al-Dosari, Nada AbuDheim, Tarfa A Alshidi, Dilek Colak, Ola Al-Habit, Ali Al-Odaib, Nadia Sakati, Brian Meyer, Pinar T Ozand, Namik Kaya Molecular Cytogenetics 2011, 4:9 (2 April 2011) Abstract \| Full text \| PDF \| PubMed
	20. 1780 Accesses	Research MLPA for confirmation of array CGH results and determination of inheritance Alison Hills, Joo Ahn, Celia Donaghue, Helen Thomas, Kathy Mann, Caroline Ogilvie Molecular Cytogenetics 2010, 3:19 (13 October 2010) Abstract \| Full text \| PDF \| PubMed
	21. 1771 Accesses	Research DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation Takema Kato, Hidehito Inagaki, Maoqing Tong, Hiroshi Kogo, Tamae Ohye, Kouji Yamada, Makiko Tsutsumi, Beverly S Emanuel, Hiroki Kurahashi Molecular Cytogenetics 2011, 4:18 (8 September 2011) Abstract \| Full text \| PDF \| PubMed
	22. 1757 Accesses	Research The use of array-CGH in a cohort of Greek children with developmental delay Emmanouil Manolakos, Annalisa Vetro, Konstantinos Kefalas, Stamatia-Maria Rapti, Eirini Louizou, Antonios Garas, George Kitsos, Lefteris Vasileiadis, Panagiota Tsoplou, Makarios Eleftheriades, Panagiotis Peitsidis, Sandro Orru, Thomas Liehr, Michael B Petersen, Loretta Thomaidis Molecular Cytogenetics 2010, 3:22 (9 November 2010) Abstract \| Full text \| PDF \| PubMed
	23. 1751 Accesses	Case report A rare case of chronic myeloid leukemia with secondary chromosomal changes including partial trisomy 17q21 to 17qter and partial monosomy of 16p13.3 Walid Al Achkar, Abdulsamad Wafa, Hasmik Mkrtchyan, Faten Moassass, Thomas Liehr Molecular Cytogenetics 2010, 3:6 (16 March 2010) Abstract \| Full text \| PDF \| PubMed
	24. 1746 Accesses	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) Abstract \| Full text \| PDF \| PubMed
	25. 1720 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