David Fitzpatrick

A syndromic form of Pierre Robin sequence is caused by 5q23 deletions encompassing FBN2 and PHAX.

K. Devriendt, H. Firth, D. Fitzpatrick, 2014, European journal of medical genetics.

Large-scale discovery of novel genetic causes of developmental disorders

Tomas W. Fitzgerald, M. Hurles, J. Barrett, 2014, Nature.

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing

Tomas W. Fitzgerald, G. J. Swaminathan, J. Danesh, 2016, Nature Genetics.

Folate and Clefts of the Lip and Palate—A U.K.-Based Case-Control Study: Part II: Biochemical and Genetic Analysis

J. Clayton-Smith, J. Little, D. Fitzpatrick, 2008, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Smoking and Orofacial Clefts: A United Kingdom–Based Case-Control Study

J. Little, P. Mossey, A. Cardy, 2004, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Folate and Clefts of the Lip and Palate—A U.K.-Based Case-Control Study: Part I: Dietary and Supplemental Folate

J. Clayton-Smith, J. Little, D. Fitzpatrick, 2008, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.