Genetics Studies of Craniofacial and Limb
ID Number 08-0513Principal Investigator(s)
Ethylin W Jabs
Department(s) or Division(s)
Genetics and Genomic Sciences
The purpose of our study is to increase our understanding of the molecular basis of human developmental malformations, especially craniofacial and limb disorders. Most of these conditions that we are studying are rare conditions occurring in less than 1 per 10,000 to 150,000 newborns. Our research group obtains informed consent for medical information and samples such as blood, skin, and tissues from patients with craniofacial and/or limb anomalies to study the genetic basis of these conditions.
Ethylin Wang Jabs
Recruiting Patients: Yes