A familial syndrome of deafness, alopecia, and hypogonadism
- 31 March 1973
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 82 (3) , 461-465
- https://doi.org/10.1016/s0022-3476(73)80121-0
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Radioimmunoassay for Human ThyrotrophinAnnals of Internal Medicine, 1971
- Plasma Metyrapone, Adrenocorticotropic Hormone, Cortisol, and Deoxycortisol LevelsArchives of internal medicine (1960), 1970
- Familial Monotropic Pituitary Gonadotropin InsufficiencyJournal of Clinical Endocrinology & Metabolism, 1968
- Radioimmunoassay for Human Luteinizing Hormone.Experimental Biology and Medicine, 1967
- Growth-Hormone Deficiency in Man: An Isolated, Recessively Inherited DefectScience, 1966
- A Sensitive Double Antibody Immunoassay for Human Growth Hormone in PlasmaNature, 1964
- Determination of Thyroxine Utilizing the Property of Protein-BindingJournal of Clinical Endocrinology & Metabolism, 1964
- Congenital Deafness Associated with OnychodystrophyJAMA Otolaryngology–Head & Neck Surgery, 1961
- Ectodermal DysplasiaAmerican Journal of Ophthalmology, 1958
- Adsorption of Urinary Gonadotrophins on KaolinExperimental Biology and Medicine, 1949