TY  - GEN
AU  - Ciara,E
AU  - Nowaczyk,M J M
AU  - Witsch-Baumgartner,M
AU  - Malunowicz,E
AU  - Popowska,E
AU  - Jezela-Stanek,A
AU  - Piotrowicz,M
AU  - Waye,J S
AU  - Utermann,G
AU  - Krajewska-Walasek,M
TI  - DHCR7 mutations and genotype-phenotype correlation in 37 Polish patients with Smith-Lemli-Opitz syndrome
SN  - 0009-9163
PY  - 2005///1114
KW  - Female
KW  - Genotype
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Male
KW  - Mutation
KW  - Oxidoreductases Acting on CH-CH Group Donors
KW  - genetics
KW  - Phenotype
KW  - Poland
KW  - Smith-Lemli-Opitz Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/j.1399-0004.2004.00350.x
ER  -