TY  - GEN
AU  - Al-Owain,M
AU  - Imtiaz,F
AU  - Shuaib,T
AU  - Edrees,A
AU  - Al-Amoudi,M
AU  - Sakati,N
AU  - Al-Hassnan,Z
AU  - Bamashmous,H
AU  - Rahbeeni,Z
AU  - Al-Ameer,S
AU  - Faqeih,E
AU  - Meyer,B
AU  - Al-Hashem,A
AU  - Garout,W
AU  - Al-Odaib,A
AU  - Rashed,M
AU  - Al-Aama,J Y
TI  - Smith-Lemli-Opitz syndrome among Arabs
SN  - 1399-0004
PY  - 2012///1113
KW  - Arabs
KW  - genetics
KW  - Child
KW  - Child, Preschool
KW  - Consanguinity
KW  - Exons
KW  - Facies
KW  - Female
KW  - Homozygote
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Male
KW  - Mutation
KW  - Oxidoreductases Acting on CH-CH Group Donors
KW  - Pedigree
KW  - Phenotype
KW  - Smith-Lemli-Opitz Syndrome
KW  - diagnosis
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/j.1399-0004.2011.01742.x
ER  -