original ) (raw )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
View PDFchevron_right
Association of recombination errors and young mother age in risk of Down Syndrome in South Indian population
IJAR Indexing
View PDFchevron_right
Down Syndrome: Parental Origin, Recombination, and Maternal Age
Vida Culic
Genetic Testing and Molecular Biomarkers, 2012
View PDFchevron_right
Etiology of Down Syndrome: Risk of Advanced Maternal Age and Altered Meiotic Recombination for Chromosome 21 Nondisjunction
Sujoy Ghosh
intechopen.com
View PDFchevron_right
Rate of recombination of chromosomes 21 in parents of children with Down syndrome
Joep Geraedts
Clinical Genetics, 2008
View PDFchevron_right
Down syndrome: genetic recombination and the origin of the extra chromosome 21
Terry Hassold
2001
View PDFchevron_right
Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study
Terry Hassold
American journal of human genetics, 1996
View PDFchevron_right
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
View PDFchevron_right
Relationship of recombination patterns and maternal age among non-disjoined chromosomes 21
Neil Lamb
Biochemical Society Transactions, 2006
View PDFchevron_right
Centromeric genotyping and direct analysis of nondisjunction in humans: Down syndrome
Terry Hassold
Chromosoma, 1998
View PDFchevron_right
Association of Genetic Polymorphisms in Genes Involved at the Branch Point of Nucleotide Biosynthesis and Remethylation with Down Syndrome Birth Risk: A Case-Control Study
Sushil Kumar Jaiswal
Journal of Molecular and Genetic Medicine, 2016
View PDFchevron_right
Gene Polymorphisms That Predispose Women for Down Syndrome Child Birth
papiya ghosh
Chromosomal Abnormalities [Working Title], 2019
View PDFchevron_right
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
View PDFchevron_right
Association between Maternal Age and Meiotic Recombination for Trisomy 21
Neil Lamb
American Journal of Human Genetics, 2005
View PDFchevron_right
Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21
Natasha Hollis
Human Genetics, 2011
View PDFchevron_right
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
View PDFchevron_right
Genomic study of the critical region of chromosome 21 associated to Down syndrome
adalberto sanchez gomez
Colombia …, 2011
View PDFchevron_right
Epidemiology of Down Syndrome: New Insight Into the Multidimensional Interactions Among Genetic and Environmental Risk Factors in the Oocyte
E. Feingold
American Journal of Epidemiology, 2011
View PDFchevron_right
Association between presenilin-1 polymorphism and maternal meiosis II errors in Down syndrome
G. Karadima
American Journal of Medical Genetics, 2000
View PDFchevron_right
Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21
E. Feingold
Human Molecular Genetics, 2014
View PDFchevron_right
Parental age and the origin of extra chromosome 21 in Down syndrome
Sujatha Madireddi
Journal of Human Genetics, 2001
View PDFchevron_right
Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16
Terry Hassold
American journal of human genetics, 1995
View PDFchevron_right
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
View PDFchevron_right
Age-Dependent Recombination Rates in Human Pedigrees
Roxanne Gendron
PLoS Genetics, 2011
View PDFchevron_right
Molecular Cytogenetic Classification of Down Syndrome and Screening of Somatic Aneuploidy in Mothers
Sushil Kumar Jaiswal
Cytogenetic and Genome Research
View PDFchevron_right
Preimplantation genetic diagnosis for couples at high risk of Down syndrome pregnancy owing to parental translocation or mosaicism
J. Cozzi
Journal of medical genetics, 1999
View PDFchevron_right
Incidence of down syndrome: Hypotheses and reality
Kanjaksha Ghosh
Indian Journal of Human Genetics, 2011
View PDFchevron_right
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
View PDFchevron_right
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
View PDFchevron_right
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
View PDFchevron_right