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

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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
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PubType: Academic Journal
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  Data: Aberrant meiotic recombination mediated by maternal RNF212, PRDM9, and SPO11 variants increases risk of chromosome 21 nondisjunction and Down syndrome birth.
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  Data: <searchLink fieldCode="AR" term="%22Pal%2C+Upamanyu%22">Pal, Upamanyu</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Halder%2C+Pinku%22">Halder, Pinku</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ganguly%2C+Agnish%22">Ganguly, Agnish</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Sarkar%2C+Sumantra%22">Sarkar, Sumantra</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ghosh%2C+Papiya%22">Ghosh, Papiya</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ghosh%2C+Sujay%22">Ghosh, Sujay</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> sgzoo@caluniv.ac.in</i>
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  Data: <searchLink fieldCode="JN" term="%22Egyptian+Journal+of+Medical+Human+Genetics%22">Egyptian Journal of Medical Human Genetics</searchLink>. 12/22/2025, Vol. 26 Issue 1, p1-21. 21p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=190408060
RecordInfo BibRecord:
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      – Type: doi
        Value: 10.1186/s43042-025-00813-5
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      – Code: eng
        Text: English
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      – TitleFull: Aberrant meiotic recombination mediated by maternal RNF212, PRDM9, and SPO11 variants increases risk of chromosome 21 nondisjunction and Down syndrome birth.
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            NameFull: Pal, Upamanyu
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            NameFull: Halder, Pinku
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            NameFull: Ganguly, Agnish
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            NameFull: Sarkar, Sumantra
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            NameFull: Ghosh, Papiya
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            NameFull: Ghosh, Sujay
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            – D: 22
              M: 12
              Text: 12/22/2025
              Type: published
              Y: 2025
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              Value: 26
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            – TitleFull: Egyptian Journal of Medical Human Genetics
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