Chassaing, N <br/><br/>
Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy-like phenotype.  [electronic resource] 

 -  American journal of medical genetics. Part A  Aug 2004 
 - 410-3 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1552-4825 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.30199  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 2<br/>Cytogenetic Analysis<br/>Female<br/>Fibrous Dysplasia, Polyostotic--genetics<br/>Humans<br/>Karyotyping<br/>Microsatellite Repeats<br/>Pedigree<br/>Phenotype