Carrier frequency of the RSH/Smith-Lemli-Opitz IVS8-1G>C mutation in African Americans

Am J Med Genet A. 2003 Jul 1;120A(1):139-41. doi: 10.1002/ajmg.a.10207.
No abstract available

Publication types

  • Letter

MeSH terms

  • Alleles
  • Black People
  • Black or African American
  • DNA Mutational Analysis
  • Gene Frequency
  • Genetic Testing
  • Genotype
  • Haplotypes
  • Heterozygote*
  • Humans
  • Intellectual Disability / genetics
  • Mutation*
  • Phenotype
  • Point Mutation
  • Smith-Lemli-Opitz Syndrome / genetics*
  • United States