Jeffrey C. Murray

Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes

D. Bick, S. Wallace, T. Mcgregor, 2014, Clinical genetics.

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

Christian Gieger, Inês Barroso, Peter Kraft, 2010, Nature Genetics.

Cloning, characterization, and mapping of the mouse homeobox gene Hmx1.

J. Murray, K. Yoshiura, R. Reiter, 1998, Genomics.

Global Oral Health Inequalities

J. Little, W. Shaw, R. Munger, 2011, Advances in dental research.

Two novel frameshift mutations in NKX2.5 result in novel features including visceral inversus and sinus venosus type ASD

J. Murray, D. Benson, Y. Watanabe, 2002, Journal of medical genetics.

Comprehensive human genetic maps: individual and sex-specific variation in recombination.

Jeffrey C. Murray, Ray White, Val C. Sheffield, 1998, American journal of human genetics.

Genetic Studies in the Nigerian Population Implicate an MSX1 Mutation in Complex Oral Facial Clefting Disorders

W. Adeyemo, M. Mansilla, C. Onwuamah, 2011, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Abnormal brain structure in adults with Van der Woude syndrome

N. Andreasen, P. Nopoulos, J. Murray, 2007, Clinical genetics.

Maternal alcohol use and risk of orofacial cleft birth defects.

R. Munger, J. Murray, T. Burns, 1996, Teratology.

The human BARX2 gene: genomic structure, chromosomal localization, and single nucleotide polymorphisms.

J. Murray, T. Hjalt, Jeffrey C. Murray, 1999, Genomics.

Refinement of the Van der Woude gene location and construction of a 3.5-Mb YAC contig and STS map spanning the critical region in 1q32-q41.

J. Murray, B. Schutte, A. Sander, 1996, Genomics.

Transforming growth factor-alpha (TGFA): genomic structure, boundary sequences, and mutation analysis in nonsyndromic cleft lip/palate and cleft palate only.

J. Murray, K. Yoshiura, T. Kawai, 1999, Genomics.