Human Genome Epidemiology Literature Finder
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Records 1 - 2 (of 2 Records) |
| Query Trace: Syndrome and NLRP7[original query] |
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| No evidence for mutations in NLRP7, NLRP2 or KHDC3L in women with unexplained recurrent pregnancy loss or infertility. Human reproduction (Oxford, England) 2015 Jan 30 (1): 232-8. Aghajanova L, Mahadevan S, Altmäe S, Stavreus-Evers A, Regan L, Sebire N, Dixon P, Fisher R A, Van den Veyver I |
| NLRP genes and their role in preeclampsia and multi-locus imprinting disorders. Journal of perinatal medicine 2017 7 46 (2): 169-173. Soellner Lukas, Kopp Kathrin Maria, Mütze Sabine, Meyer Robert, Begemann Matthias, Rudnik Sabine, Rath Werner, Eggermann Thomas, Zerres Kla |
- Page last reviewed:Feb 1, 2024
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