View in EDS HTML Full Text PDF Full Text

Aberrant meiotic recombination mediated by maternal RNF212, PRDM9, and SPO11 variants increases risk of chromosome 21 nondisjunction and Down syndrome birth.

Saved in:

Bibliographic Details
Title:	Aberrant meiotic recombination mediated by maternal RNF212, PRDM9, and SPO11 variants increases risk of chromosome 21 nondisjunction and Down syndrome birth.
Authors:	Pal, Upamanyu¹ (AUTHOR), Halder, Pinku¹ (AUTHOR), Ganguly, Agnish¹ (AUTHOR), Sarkar, Sumantra² (AUTHOR), Ghosh, Papiya³ (AUTHOR), Ghosh, Sujay¹ (AUTHOR) sgzoo@caluniv.ac.in
Source:	Egyptian Journal of Medical Human Genetics. 12/22/2025, Vol. 26 Issue 1, p1-21. 21p.
Database:	Academic Search Ultimate
Full text is not displayed to guests. Login for full access.

Description
ISSN:	11108630
DOI:	10.1186/s43042-025-00813-5