Polymorphisms of folate metabolism regulators increase risk of meiosis II nondisjunction of chromosome 21 in oocyte
Author:
Funder
Department of Science and Technology
Govt. of West Bengal
UGC-UPE II
DST-FIST
UGC-PURSE
University of Calcutta
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
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1. Association Study of Polymorphisms in Folate Metabolism and Mothers of Down Syndrome Offsprings in the Southwest of Iran;Jundishapur Journal of Chronic Disease Care;2024-01-20
2. Association of C677T and A1298C polymorphisms of the MTHFR gene with maternal risk for Down syndrome: A meta-analysis of case-control studies;Mutation Research/Reviews in Mutation Research;2023-07
3. Genetic aetiology of Down syndrome birth: novel variants of maternal DNMT3B and RFC1 genes increase risk of meiosis II nondisjunction in the oocyte;Molecular Genetics and Genomics;2022-11-30
4. Understanding etiology of chromosome 21 nondisjunction from gene × environment models;Scientific Reports;2021-11-17
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