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

Am J Med Genet. 1993 Mar 1;45(5):565-9. doi: 10.1002/ajmg.1320450508.

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.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alleles
  • Asian People / genetics
  • Black People / genetics
  • Child
  • Cleft Lip / genetics*
  • Cleft Palate / genetics
  • DNA / genetics
  • Gene Frequency
  • Genetic Linkage
  • Humans
  • Models, Genetic
  • Polymorphism, Restriction Fragment Length
  • Transforming Growth Factor alpha / genetics*
  • White People / genetics

Substances

  • Transforming Growth Factor alpha
  • DNA