Sex chromosomes-linked single-gene disorders involved in human infertility
- 25 October 2018
- journal article
- review article
- Published by Elsevier in European Journal of Medical Genetics
- Vol. 62 (9), 103560
- https://doi.org/10.1016/j.ejmg.2018.10.012
Abstract
No abstract availableThis publication has 151 references indexed in Scilit:
- Hypogonadotropic hypogonadism in subjects with DAX1 mutationsMolecular and Cellular Endocrinology, 2011
- Genomic analysis using high-resolution single-nucleotide polymorphism arrays reveals novel microdeletions associated with premature ovarian failureFertility and Sterility, 2011
- Expanding the Phenotype and Genotype of Female GnRH DeficiencyJournal of Clinical Endocrinology & Metabolism, 2011
- Mendelian genetics of male infertilityAnnals of the New York Academy of Sciences, 2010
- Vasa genes: Emerging roles in the germ line and in multipotent cellsBioEssays, 2010
- BMP15 Mutations Associated With Primary Ovarian Insufficiency Cause a Defective Production of Bioactive ProteinHuman Mutation, 2009
- Alterations in the expression, structure and function of progesterone receptor membrane component-1 (PGRMC1) in premature ovarian failureHuman Molecular Genetics, 2008
- An evolutionary perspective on Y‐chromosomal variation and male infertilityInternational Journal of Andrology, 2008
- Disruption of POF1B Binding to Nonmuscle Actin Filaments Is Associated with Premature Ovarian FailureAmerican Journal of Human Genetics, 2006
- A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motifNature, 1990