Smith-Lemli-Opitz syndrome: carrier frequency and spectrum of DHCR7 mutations in Canada
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Overview
status
publication date
- June 1, 2002
has subject area
- 06 Biological Sciences (FoR)
- 11 Medical and Health Sciences (FoR)
- Canada (MeSH)
- Gene Frequency (MeSH)
- Genetic Carrier Screening (MeSH)
- Genetics & Heredity (Science Metrix)
- Humans (MeSH)
- Mutation (MeSH)
- Oxidoreductases (MeSH)
- Oxidoreductases Acting on CH-CH Group Donors (MeSH)
- Polymorphism, Single Nucleotide (MeSH)
- Smith-Lemli-Opitz Syndrome (MeSH)
published in
- Journal of Medical Genetics Journal