Primary hypogonadism and partial alopecia in three sibs with Müllerian hypoplasia in the affected females
- 1 November 1985
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 22 (3) , 619-622
- https://doi.org/10.1002/ajmg.1320220322
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Familial gonadal germinative failure: endocrine and human leukocyte antigen studiesFertility and Sterility, 1983
- A newly recognized neuroectodermal syndrome of familial alopecia, anosmia, deafness, and hypogonadismAmerican Journal of Medical Genetics, 1983
- A syndrome of hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness, and ECG abnormalities.Journal of Medical Genetics, 1983
- Three Siblings with Premature Gonadal FailureFertility and Sterility, 1979
- Congenital Absence of the VaginaAnnals of Internal Medicine, 1976
- Endocrine Studies in Sertoli-Cell-Only SyndromeJournal of Urology, 1976
- Gonadotropin Response to Luteinizing Hormone-Releasing Hormone in Men with Germinal AplasiaJournal of Clinical Endocrinology & Metabolism, 1974
- The XY Gonadal Agenesis SyndromeJournal of Medical Genetics, 1973
- Hypertension With Adrenal, Genital, Renal Defects, and DeafnessArchives of internal medicine (1960), 1973
- A familial syndrome of deafness, alopecia, and hypogonadismThe Journal of Pediatrics, 1973