A case of Albright's hereditary osteodystrophy-like syndrome complicated by several endocrinopathies: Normal Gsα gene and chromosome 2q37

Journal of Clinical Endocrinology and Metabolism

Volumn 83, Issue 5, 1998, Pages 1563-1565

  Sakaguchi, Hidenobu ^a   Sanke, Tokio ^a   Ohagi, Shinya ^a   Iiri, Taroh ^b,c   Nanjo, Kishio ^a  

^a WAKAYAMA MEDICAL UNIVERSITY   (Japan)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c UNIVERSITY OF TOKYO   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; GLUCAGON; GROWTH HORMONE; GROWTH HORMONE RELEASING FACTOR; INSULIN; PARATHYROID HORMONE; VASOPRESSIN;

ADULT; ALBRIGHT SYNDROME; ARTICLE; BRACHYDACTYLY; CASE REPORT; CHROMOSOME 2Q; DEXAMETHASONE SUPPRESSION TEST; DIABETES INSIPIDUS; DISEASE ASSOCIATION; ENDOCRINE DISEASE; FEMALE; GENE FUNCTION; GROWTH HORMONE BLOOD LEVEL; HORMONE RESISTANCE; HUMAN; INSULIN RESISTANCE; INTRAVENOUS DRUG ADMINISTRATION; MENTAL DEFICIENCY; NON INSULIN DEPENDENT DIABETES MELLITUS; OBESITY; PRIORITY JOURNAL; SHORT STATURE; VASOPRESSIN BLOOD LEVEL;

EID: 0031723981     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jcem.83.5.4781     Document Type: Article

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