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On the origin of trisomy 21 Down syndrome
Maj A Hultén, Suketu D Patel, Maira Tankimanova, Magnus Westgren, Nikos Papadogiannakis, Anna Maria Jonsson, Erik Iwarsson
Mol Cytogenet. 2008; 1: 21. Published online 2008 September 18. doi: 10.1186/1755-8166-1-21
PMCID:
PMC2564957
Abstract Full Text PDF–478K
 Is Cited by the Following 13 Articles in this Archive:
A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation
Khaled K Abu-Amero, Ali M Hellani, Mustafa A Salih, Mohammad Z Seidahmed, Tageldin S Elmalik, Ghassan Zidan, Thomas M Bosley
BMC Med Genet. 2010; 11: 135. Published online 2010 September 21. doi: 10.1186/1471-2350-11-135
PMCID:
PMC2946294
Abstract Full Text PDF–830K Supplementary Material
Somatic Genomic Variations in Early Human Prenatal Development
Caroline Robberecht, Evelyne Vanneste, Anne Pexsters, Thomas D’Hooghe, Thierry Voet, Joris R. Vermeesch
Curr Genomics. 2010 September; 11(6): 397–401. doi: 10.2174/138920210793175967
PMCID:
PMC3018719
Abstract Full Text PDF–112K
Germinal and Somatic Trisomy 21 Mosaicism: How Common is it, What are the Implications for Individual Carriers and How Does it Come About?
Maj A. Hultén, Jon Jonasson, Ann Nordgren, Erik Iwarsson
Curr Genomics. 2010 September; 11(6): 409–419. doi: 10.2174/138920210793176056
PMCID:
PMC3018721
Abstract Full Text PDF–264K
Molecular Cytogenetic Diagnosis and Somatic Genome Variations
S.G Vorsanova, Y.B. Yurov, I.V. Soloviev, I.Y. Iourov
Curr Genomics. 2010 September; 11(6): 440–446. doi: 10.2174/138920210793176010
PMCID:
PMC3018725
Abstract Full Text PDF–150K
Parental and Grandparental Ages in the Autistic Spectrum Disorders: A Birth Cohort Study
Jean Golding, Colin Steer, Marcus Pembrey
PLoS One. 2010; 5(4): e9939. Published online 2010 April 1. doi: 10.1371/journal.pone.0009939
PMCID:
PMC2848579
Abstract Full Text PDF–325K
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
Mol Cytogenet. 2010; 3: 4. Published online 2010 February 23. doi: 10.1186/1755-8166-3-4
PMCID:
PMC2848052
Abstract Full Text PDF–304K
Human interphase chromosomes: a review of available molecular cytogenetic technologies
Svetlana G Vorsanova, Yuri B Yurov, Ivan Y Iourov
Mol Cytogenet. 2010; 3: 1. Published online 2010 January 11. doi: 10.1186/1755-8166-3-1
PMCID:
PMC2830939
Abstract Full Text PDF–1.8M
Maternal age and chromosomally abnormal pregnancies: what we know and what we wish we knew
Terry Hassold, Patricia Hunt
Curr Opin Pediatr. Author manuscript; available in PMC 2010 December 1.
Published in final edited form as: Curr Opin Pediatr. 2009 December; 21(6): 703–708. doi: 10.1097/MOP.0b013e328332c6ab
PMCID:
PMC2894811
Abstract Full Text PDF–712K
GIN'n'CIN hypothesis of brain aging: deciphering the role of somatic genetic instabilities and neural aneuploidy during ontogeny
Yuri B Yurov, Svetlana G Vorsanova, Ivan Y Iourov
Mol Cytogenet. 2009; 2: 23. Published online 2009 November 25. doi: 10.1186/1755-8166-2-23
PMCID:
PMC2787505
Abstract Full Text PDF–1.9M
Oogenesis and cell death in human prenatal ovaries: what are the criteria for oocyte selection?
G.M. Hartshorne, S. Lyrakou, H. Hamoda, E. Oloto, F. Ghafari
Mol Hum Reprod. 2009 December; 15(12): 805–819. Published online 2009 July 7. doi: 10.1093/molehr/gap055
PMCID:
PMC2776471
Abstract Full Text PDF–726K
UNDERSTANDING WHAT DETERMINES THE FREQUENCY AND PATTERN OF HUMAN GERMLINE MUTATIONS
Norman Arnheim, Peter Calabrese
Nat Rev Genet. Author manuscript; available in PMC 2010 January 1.
Published in final edited form as: Nat Rev Genet. 2009 July; 10(7): 478–488. doi: 10.1038/nrg2529
PMCID:
PMC2744436
Abstract Full Text PDF–1.0M
Chromosomal mosaicism goes global
Ivan Y Iourov, Svetlana G Vorsanova, Yuri B Yurov
Mol Cytogenet. 2008; 1: 26. Published online 2008 November 25. doi: 10.1186/1755-8166-1-26
PMCID:
PMC2612668
Abstract Full Text PDF–497K
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