Linglart, Agnès <br/><br/>
GNAS1 lesions in pseudohypoparathyroidism Ia and Ic: genotype phenotype relationship and evidence of the maternal transmission of the hormonal resistance.  [electronic resource] 

 -  The Journal of clinical endocrinology and metabolism  Jan 2002 
 - 189-97 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article 
<br/><br/><label>ISSN: </label>0021-972X 
<br/><br/><label>Standard No.: </label>10.1210/jcem.87.1.8133  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Alleles<br/>Child<br/>Child, Preschool<br/>Female<br/>Fibrous Dysplasia, Polyostotic--genetics<br/>GTP-Binding Protein alpha Subunits, Gs--deficiency<br/>Genotype<br/>Humans<br/>Hypocalcemia--genetics<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Middle Aged<br/>Mutation<br/>Pedigree<br/>Phenotype<br/>Pseudohypoparathyroidism--blood