A case of Albright's hereditary osteodystrophy-like syndrome complicated by several endocrinopathies: normal Gs alpha gene and chromosome 2q37. [electronic resource]
Producer: 19980604Description: 1563-5 p. digitalISSN:- 0021-972X
- Adult
- Chromosomes, Human, Pair 2
- DNA Mutational Analysis
- Diabetes Insipidus -- complications
- Diabetes Mellitus, Type 2 -- complications
- Endocrine System Diseases -- complications
- Female
- Fibrous Dysplasia, Polyostotic -- complications
- GTP-Binding Protein alpha Subunits, Gs -- genetics
- Human Growth Hormone -- deficiency
- Humans
- Insulin Resistance
- Karyotyping
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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