Abstract 7: Novel Stem Cell Model of Frontonasal Dysplasia derived from Pedigree with ALX1-Mutation
Janina Kueper(University of Bonn), Eric C. Liao(Children's Hospital of Philadelphia), Victoria Perroni(Brigham and Women's Hospital), Yevgenya Grinblatt(University of Wisconsin–Madison), Jonathan Pini(Massachusetts General Hospital), Nikkola Carmichael(Boston University), Kana Ishii(Center For Reconstructive Urethral Surgery), Yiyuan Hu(Massachusetts General Hospital), Megan Rebello(Massachusetts General Hospital), Richard L. Maas(Brigham and Women's Hospital), Nikhil Sobti
Cited by 0
Related Papers
Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development
|Nature Genetics|1994|1.3k
Sonic hedgehog regulates growth and morphogenesis of the tooth
|Development|2000|804
Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
|Nature Genetics|2000|740
Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia
|Nature Genetics|1999|718