Sakaguchi, H <br/><br/>
A case of Albright's hereditary osteodystrophy-like syndrome complicated by several endocrinopathies: normal Gs alpha gene and chromosome 2q37.  [electronic resource] 

 -  The Journal of clinical endocrinology and metabolism  May 1998 
 - 1563-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0021-972X 
<br/><br/><label>Standard No.: </label>10.1210/jcem.83.5.4781  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Chromosomes, Human, Pair 2<br/>DNA Mutational Analysis<br/>Diabetes Insipidus--complications<br/>Diabetes Mellitus, Type 2--complications<br/>Endocrine System Diseases--complications<br/>Female<br/>Fibrous Dysplasia, Polyostotic--complications<br/>GTP-Binding Protein alpha Subunits, Gs--genetics<br/>Human Growth Hormone--deficiency<br/>Humans<br/>Insulin Resistance<br/>Karyotyping