Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Trisomy and PRDM9[original query] |
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Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction. Human genetics 2012 Sep 131 (9): 1519-24. Borel Christelle, Cheung Fanny, Stewart Helen, Koolen David A, Phillips Christopher, Thomas N Simon, Jacobs Patricia A, Eliez Stephan, Sharp Andrew |
Variation in the Zinc Finger of PRDM9 is Associated with the Absence of Recombination along Nondisjoined Chromosomes 21 of Maternal Origin. Journal of Down Syndrome & chromosome abnormalities 2016 Dec 2 (2): . Oliver Tiffany Renee, Middlebrooks Candace, Harden Ariel, Scott Nyeisha, Johnson Blair, Jones Jillian, Walker Christin, Wilkerson Corinthia, Saffold Sha-Hanna, Akinseye Abisola, Smith Tunde, Feingold Eleanor, Sherman Stephanie |
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