Contemporary issues in primary amenorrhea
- 1 June 2003
- journal article
- review article
- Published by Elsevier in Obstetrics and Gynecology Clinics of North America
- Vol. 30 (2) , 287-302
- https://doi.org/10.1016/s0889-8545(03)00027-5
Abstract
No abstract availableKeywords
This publication has 46 references indexed in Scilit:
- A Novel Mutation in the FSH Receptor Inhibiting Signal Transduction and Causing Primary Ovarian FailureJournal of Clinical Endocrinology & Metabolism, 2002
- A Human Homologue of the Drosophila melanogaster diaphanous Gene Is Disrupted in a Patient with Premature Ovarian Failure: Evidence for Conserved Function in Oogenesis and Implications for Human SterilityAmerican Journal of Human Genetics, 1998
- Mutations in gonadotropin-releasing hormone receptor gene cause hypogonadotropic hypogonadismNature Genetics, 1998
- Congenital absence of the uterus and vagina (CAUV) is not associated with the N314D allele of the Galactose-1-Phosphate Uridyl Transferase (GALT) geneJournal of the Society for Gynecologic Investigation, 1998
- Delayed Puberty and Hypogonadism Caused by Mutations in the Follicle-Stimulating Hormone β-Subunit GeneNew England Journal of Medicine, 1997
- A new variant of the cytochrome P450c17 (CYP17) gene mutation in three patients with 17 α‐hydroxylase deficiencyAnnals of Human Genetics, 1997
- Congenital absence of the uterus and vagina is not commonly transmitted as a dominant genetic trait: Outcomes of surrogate pregnanciesFertility and Sterility, 1997
- Eleven X Chromosome Breakpoints Associated with Premature Ovarian Failure (POF) Map to a 15-Mb YAC Contig Spanning Xq21Genomics, 1997
- Evidence That the SRY Protein Is Encoded by a Single Exon on the Human Y ChromosomeGenomics, 1993
- Camptomelic dwarfism associated with XY‐gonadal dysgenesis and chromosome anomaliesClinical Genetics, 1978