Association between alleles of the transforming growth factor‐alpha locus and the occurrence of cleft lip

Russell Sassani(Children's Hospital of Philadelphia), Scott P. Bartlett(Children's Hospital of Philadelphia), Hongshu Feng(University of Pennsylvania), Audrey J. Goldner-Sauvé(University of Pennsylvania), Asifa K. Haq(University of Pennsylvania), Kenneth H. Buetow(Fox Chase Cancer Center), David L. Gasser(University of Pennsylvania)
American Journal of Medical Genetics
March 1, 1993
Cited by 68

Abstract

DNA samples from 100 patients with cleft lip with or without cleft palate (CL/P) were compared with those of 98 unaffected control individuals with respect to transforming growth factor alpha (TGFA) genotypes. Among the Caucasians in this population (83 CL/P, 84 controls), there was a significant difference in the restriction fragment length polymorphisms (RFLPs) observed after digestion with TaqI (chi 2 = 4.68, P = 0.03). The frequency of the C2 allele in the Caucasian CL/P population was 0.169, whereas that in the control group was 0.089. When the data for Caucasians, African-Americans, and Asians were examined jointly, the chi 2 value for the pooled sample was 5.08 (P = 0.02). This confirms the hypothesis of Ardinger et al. [1989, Am J Hum Genet, 45:348-353] that TFGA itself or a closely linked gene contributes to the development of CL/P in humans.


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