Developmental Dysplasia of the Hip: Linkage Mapping and Whole Exome Sequencing Identify a Shared Variant in CX 3 CR 1 in All Affected Members of a Large Multigeneration Family

✍ Scribed by Feldman, George J; Parvizi, Javad; Levenstien, Mark; Scott, Kathryn; Erickson, Jill A; Fortina, Paolo; Devoto, Marcella; Peters, Christopher L

• Book ID: 127313607
• Publisher: American Society for Bone and Mineral Research
• Year: 2013
• Tongue: English
• Weight: 628 KB
• Volume: 28
• Category: Article
• ISSN: 0884-0431
• DOI: 10.1002/jbmr.1999