Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Infertility and HOXA10[original query] |
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Homeobox HOXA10 gene analysis in cryptorchidism. Journal of pediatric endocrinology & metabolism : JPEM 2004 Jan 17 (1): 41-5. Bertini Veronica, Bertelloni Silvano, Valetto Angelo, Lala Roberto, Foresta Carlo, Simi Pao |
HOXA10 mutations in congenital absence of uterus and vagina. Fertility and sterility 2008 Feb 89 (2): 325-30. Lalwani Sasmira, Wu Hsin-hung, Reindollar Richard H, Gray Mark |
HOXA10 and HOXA13 sequence variations in human female genital malformations including congenital absence of the uterus and vagina. Gene 2013 Jan . Ekici AB, Strissel PL, Oppelt PG, Renner SP, Brucker S, Beckmann MW, Strick R |
Single nucleotide polymorphisms associated with nonsyndromic cryptorchidism in Mexican patients. Andrologia 2018 Feb 50 (1): . Chávez-Saldaña M, Vigueras-Villaseñor R M, Yokoyama-Rebollar E, Landero-Huerta D A, Rojas-Castañeda J C, Taja-Chayeb L, Cuevas-Alpuche J O, Zambrano |
Insights from genomic studies on the role of sex steroids in the aetiology of endometriosis. Reproduction & fertility 2022 5 3 (2): R51-R65. Saunders Philippa T |
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