Recombination across the centromere of disjoined and non-disjoined chromosome 21 (original) (raw)
Patterns of Meiotic Recombination on the Long Arm of Human Chromosome 21
Stylianos Antonarakis
Genome Research, 2000
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Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21
Natasha Hollis
Human Genetics, 2011
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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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Relationship of recombination patterns and maternal age among non-disjoined chromosomes 21
Neil Lamb
Biochemical Society Transactions, 2006
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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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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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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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Variation in MLH1 distribution in recombination maps for individual chromosomes from human males
Thomas Liehr
Human Molecular Genetics, 2006
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DSLINK: a computer program for gene-centromere linkage analysis in families with a trisomic offspring
Susan Blanton
American journal of human genetics, 1987
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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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Crossing over and chromosome 21 nondisjunction: A study of 60 families
Maurizia Baldi
American Journal of Medical Genetics, 2005
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Human Male Recombination Maps for Individual Chromosomes
Thomas Liehr
The American Journal of Human Genetics, 2004
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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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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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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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Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21
E. Feingold
Human Molecular Genetics, 2014
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A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination
Stylianos Antonarakis
The American Journal of Human Genetics, 1995
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Analysis of recombination along chromosome 21 during human female pachytene stage
Ignasi Roig, J. Barbero
Reproductive BioMedicine Online, 2009
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Parental Origin and Mechanism of Formation of de novo Chromosome Abnormalities : 25 Cases of Numerical and Structural Abnormalities Determined by Restriction Fragment Length Polymorphisms
Han-Xiang Deng
Acta Medica Nagasakiensia, 1991
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Variation in meiotic recombination frequencies among human males
Kiril Trpkov
Human Genetics, 2005
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Discontinuities and unsynapsed regions in meiotic chromosomes have a trans effect on meiotic recombination of some chromosomes in human males
Thomas Liehr
Cytogenetic and Genome Research, 2007
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Chromosome Information Service (CIS), XVII
Bani Gajra
The Nucleus, 2011
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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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Genetic and Physical Analyses of the Centromeric and Pericentromeric Regions of Human Chromosome 5: Recombination across 5cen
Alphonse Calenda
Genomics, 1999
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Variation in Human Meiotic Recombination
Audrey Lynn
Annual Review of Genomics and Human Genetics, 2004
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