Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Down Syndrome and DNMT3B[original query] |
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DNMT3B promoter polymorphisms and maternal risk of birth of a child with Down syndrome. Human reproduction (Oxford, England) 2012 Oct . Coppedè F, Bosco P, Tannorella P, Romano C, Antonucci I, Stuppia L, Romano C, Migliore L |
Maternal risk for down syndrome and polymorphisms in the promoter region of the DNMT3B gene: a case-control study. Birth defects research. Part A, Clinical and molecular teratology 2015 Apr 103 (4): 299-305. Jaiswal Sushil Kumar, Sukla Krishna Kishore, Kumari Neha, Lakhotia Anjali Rani, Kumar Ashok, Rai Amit Kum |
DNA (cytosine-5)-methyltransferase 3B (DNMT 3B) polymorphism and risk of Down syndrome offspring. Saudi journal of biological sciences 2018 Jan 25 (1): 101-104. Moura Cláudia Melo de, Bastos Pedro Ribeiro, Ribeiro Julyana S V, Ribeiro Márcia Gonçalves, Amorim Márcia Rodrigues, Costa-Lima Marcelo Agui |
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 : MGG 2022 11 298 (1): 293-313. Halder Pinku, Pal Upamanyu, Ganguly Agnish, Ghosh Papiya, Ray Anirban, Sarkar Sumantra, Ghosh Suj |
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