Genetics Studies of Craniofacial and Limb

ID Number 08-0513

Principal 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.

Contact Information
Ethylin Wang Jabs
(212) 241-3504

Recruiting Patients: Yes