Crossing over and chromosome 21 nondisjunction: A study of 60 families (original) (raw)
Rate of recombination of chromosomes 21 in parents of children with Down syndrome
Joep Geraedts
Clinical Genetics, 2008
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Centromeric genotyping and direct analysis of nondisjunction in humans: Down syndrome
Terry Hassold
Chromosoma, 1998
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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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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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Down syndrome: genetic recombination and the origin of the extra chromosome 21
Terry Hassold
2001
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Study of the origin of nondisjunction in a family with two cases of Down syndrome using cytogenetic and molecular polymorphisms
Christine Van Broeckhoven
American Journal of Medical Genetics, 2005
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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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Down Syndrome: Parental Origin, Recombination, and Maternal Age
Vida Culic
Genetic Testing and Molecular Biomarkers, 2012
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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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Meiotic crossing-over in nondisjoined chromosomes of children with trisomy 21 and a congenital heart defect
Richard Wyse
American journal of human genetics, 1993
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High efficiency in the attribution of parental origin of non-disjunction in trisomy 21 by both cytogenetic and molecular polymorphisms
Nicoletta Sacchi
Human Genetics, 1988
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No evidence for a paternal interchromosomal effect from analysis of the origin of nondisjunction in Down syndrome patients with concomitant familial chromosome rearrangements
SEHER BAŞARAN
American journal of human genetics, 1992
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Chromosome 21 non-disjunction and Down syndrome birth in an Indian cohort: analysis of incidence and aetiology from family linkage data
Sujoy Ghosh
Genetics …, 2010
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Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome
Stylianos Antonarakis
American journal of human genetics, 1992
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Discerning non-disjunction in down syndrome patients by means of gluk1-(agat) n and d21s2055-(gata) n microsatellites on chromosome 21
Swagata Sinha
Indian Journal of Human Genetics, 2012
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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
Dalila Camelo Salamanca
Biomedica, 2007
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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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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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Association of recombination errors and young mother age in risk of Down Syndrome in South Indian population
IJAR Indexing
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Cytogenetic and epidemiological findings in Down syndrome, England and Wales 1989 to 1993. National Down Syndrome Cytogenetic Register and the Association of Clinical Cytogeneticists
E. Alberman
Journal of Medical Genetics, 1996
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No significant effect of monosomy for distal 21q22.3 on the Down syndrome phenotype in "mirror" duplications of chromosome 21
J. Delabar, Christine Verellen
American journal of human genetics, 1992
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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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Parental age and the origin of extra chromosome 21 in Down syndrome
Sujatha Madireddi
Journal of Human Genetics, 2001
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Trisomy 21: Origin of non-disjunction
Amalia Castillo
Human Genetics, 1982
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Cytogenetic Analysis in Down Syndrome
Preetha Tilak
Int J Hum …, 2010
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Maternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: a report from the Atlanta and National Down Syndrome Projects
Leslie Oleary, Paul Romitti
Human Genetics, 2009
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Cytogenetic findings at Down syndrome and their correlation with clinical findings
Amra Catovic
Bosnian journal of basic medical sciences / Udruženje basičnih mediciniskih znanosti = Association of Basic Medical Sciences, 2005
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Maternal age and origin of non-disjunction in trisomy 21
Ségolène Ayme
Journal of Medical Genetics, 1980
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Risk factors for nondisjunction of trisomy 21
Neil Lamb
Cytogenetic and Genome Research, 2005
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Chromosome 21 and Down syndrome: from genomics to pathophysiology
Stylianos Antonarakis
Nature Reviews Genetics, 2004
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Cytogenetic Analysis of Down Syndrome
Editor International Journal of Clinical and Biomedical Resaerch (IJCBR)
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Analysis of DNA haplotypes suggests a genetic predisposition to trisomy 21 associated with DNA sequences on chromosome 21
Achyut Patel
Proceedings of the National Academy of Sciences, 1985
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