Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21 (original) (raw)
Relationship of recombination patterns and maternal age among non-disjoined chromosomes 21
Neil Lamb
Biochemical Society Transactions, 2006
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Association between Maternal Age and Meiotic Recombination for Trisomy 21
Neil Lamb
American Journal of Human Genetics, 2005
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Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombination
Simone Schuffenhauer
Human Molecular Genetics, 1998
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Lack of evidence for association of meiotic nondisjunction with particular DNA haplotypes on chromosome 21
Nicoletta Sacchi
Proceedings of the National Academy of Sciences, 1988
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Patterns of Meiotic Recombination on the Long Arm of Human Chromosome 21
Stylianos Antonarakis
Genome Research, 2000
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Recombination across the centromere of disjoined and non-disjoined chromosome 21
Anne-marie Laurent
Human Molecular Genetics, 2003
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Strong correlation between meiotic crossovers and haplotype structure in a 2.5-Mb region on the long arm of chromosome 21
Richeng Gao, Guohong Hu
Genome Research, 2005
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The meiotic stage of nondisjunction in trisomy 21: Determination by using DNA polymorphisms
Stylianos Antonarakis
The American Journal of Human Genetics, 1992
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A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21
Terry Hassold
PLOS Genetics, 2019
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Variation in the Zinc Finger of PRDM9 is Associated with the Absence of Recombination along Nondisjoined Chromosomes 21 of Maternal Origin
Abisola Akinseye
Journal of Down Syndrome & chromosome abnormalities, 2016
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Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21
E. Feingold
Human Molecular Genetics, 2014
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Discontinuities and unsynapsed regions in meiotic chromosomes have a cis effect on meiotic recombination patterns in normal human males
Kiril Trpkov
Human Molecular Genetics, 2005
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Nondisjunction in trisomy 21: Origin and mechanisms
Dr Jagdish kandpal
Cytogenetic and Genome Research, 2000
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Crossing over and chromosome 21 nondisjunction: A study of 60 families
Maurizia Baldi
American Journal of Medical Genetics, 2005
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Analysis of meiotic recombination in 22q11.2, a region that frequently undergoes deletions and duplications
Juan la Torre
BMC Medical Genetics, 2007
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Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16
Terry Hassold
American journal of human genetics, 1995
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Etiology of Down syndrome: Evidence for consistent association among altered meiotic recombination, nondisjunction, and maternal age across populations
Sujoy Ghosh
American Journal of Medical Genetics Part A, 2009
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Effect of meiotic recombination on the production of aneuploid gametes in humans
Neil Lamb
Cytogenetic and Genome Research, 2005
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Etiology of Down Syndrome: Risk of Advanced Maternal Age and Altered Meiotic Recombination for Chromosome 21 Nondisjunction
Sujoy Ghosh
intechopen.com
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Parental origin, nondisjunction, and recombination of the extra chromosome 21 in Down syndrome: a study in a sample of the Colombian population
Luis Valero Quintero
Biomedica, 2007
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Origen parental, estado de no disyunción y recombinación meiótica del cromosoma 21 extra en el síndrome de Down: estudio en una muestra de población colombiana
Nelson Ramirez
Biomédica, 2007
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Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19
Kevin Murphy Hansen
American journal of human genetics, 1993
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Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysis. Am J Hum Genet
Jean-louis Blouin
The American Journal of Human Genetics
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High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions
Malgorzata Krajewska-Walasek
Human Molecular Genetics, 1998
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Association of recombination errors and young mother age in risk of Down Syndrome in South Indian population
IJAR Indexing
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Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21
Lee Shulman
Journal of Medical Genetics, 1995
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The etiology of Down syndrome: Maternal MCM9 polymorphisms increase risk of reduced recombination and nondisjunction of chromosome 21 during meiosis I within oocyte
papiya ghosh
PLOS Genetics, 2021
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