Publications by authors named "Chad T Morgan"

Claim this Profile
A
Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes.
Ravinesh A Kumar, David B Everman, Chad T Morgan, Anne Slavotinek, Charles E Schwartz

BMC Med Genet· July 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non-syndromic split-hand/foot malformation.
David B Everman, Chad T Morgan, Robert Lyle, Mary E Laughridge, Michael J Bamshad

Am J Med Genet A· July 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24.
Xavier J de Mollerat, Fiorella Gurrieri, Chad T Morgan, Eugenio Sangiorgi, David B Everman

Hum Mol Genet· August 2003

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis