Association between MTHFR C677T and A1298C gene polymorphisms and maternal risk for Down syndrome: A protocol for systematic review and/or meta-analysis

BACKGROUND: Down syndrome (DS) is one of the most common chromosomal abnormalities among live-born babies and one of the best-known intellectual disability disorders in humans. Errors leading to trisomy 21 are primarily arising from defects in chromosomal segregation during maternal meiosis (about 8...

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Detalles Bibliográficos
Autores principales: Ginani, Carla Talita Azevedo, da Luz, Jefferson Romáryo Duarte, Silva, Saulo Victor e, Coppedè, Fabio, Almeida, Maria das Graças
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
5500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8772651/
https://www.ncbi.nlm.nih.gov/pubmed/35060496
http://dx.doi.org/10.1097/MD.0000000000028293

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8772651/
https://www.ncbi.nlm.nih.gov/pubmed/35060496
http://dx.doi.org/10.1097/MD.0000000000028293

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