TY  - GEN
AU  - Waye,J S
AU  - Nakamura,L M
AU  - Eng,B
AU  - Hunnisett,L
AU  - Chitayat,D
AU  - Costa,T
AU  - Nowaczyk,M J M
TI  - Smith-Lemli-Opitz syndrome: carrier frequency and spectrum of DHCR7 mutations in Canada
SN  - 1468-6244
PY  - 2002///0708
KW  - Canada
KW  - Gene Frequency
KW  - Genetic Carrier Screening
KW  - Humans
KW  - Mutation
KW  - Oxidoreductases
KW  - genetics
KW  - Oxidoreductases Acting on CH-CH Group Donors
KW  - Polymorphism, Single Nucleotide
KW  - Smith-Lemli-Opitz Syndrome
N1  - Publication Type: Letter; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1136/jmg.39.6.e31
ER  -