authors
- Wright, Brooke S
- Nwokoro, Ngozi A
- Wassif, Christopher A
- Porter, Forbes D
- Waye, John
- Eng, Barry
- Nowaczyk, Malgorzata
Carrier frequency of the RSH/Smith‐Lemli‐Opitz IVS8‐1G>C mutation in African Americans
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Overview
status
publication date
- July 2003
has subject area
- 0604 Genetics (FoR)
- 1103 Clinical Sciences (FoR)
- Alleles (MeSH)
- Black People (MeSH)
- Black or African American (MeSH)
- DNA Mutational Analysis (MeSH)
- Gene Frequency (MeSH)
- Genetic Testing (MeSH)
- Genotype (MeSH)
- Haplotypes (MeSH)
- Heterozygote (MeSH)
- Humans (MeSH)
- Intellectual Disability (MeSH)
- Mutation (MeSH)
- Phenotype (MeSH)
- Point Mutation (MeSH)
- Smith-Lemli-Opitz Syndrome (MeSH)
- United States (MeSH)