TY  - GEN
AU  - Saadi,Abdelkrim
AU  - Borck,Guntram
AU  - Boddaert,Nathalie
AU  - Chekkour,Mohamed Chahine
AU  - Imessaoudene,Belaïd
AU  - Munnich,Arnold
AU  - Colleaux,Laurence
AU  - Chaouch,Malika
TI  - Compound heterozygous ASPM mutations associated with microcephaly and simplified cortical gyration in a consanguineous Algerian family
SN  - 1878-0849
PY  - 2009///1102
KW  - Algeria
KW  - Birth Weight
KW  - Cerebral Cortex
KW  - abnormalities
KW  - Child
KW  - Consanguinity
KW  - Family
KW  - Female
KW  - Haplotypes
KW  - Heterozygote
KW  - Humans
KW  - Intellectual Disability
KW  - genetics
KW  - Male
KW  - Microcephaly
KW  - diagnostic imaging
KW  - Mutation
KW  - Nerve Tissue Proteins
KW  - Pedigree
KW  - Radiography
KW  - Siblings
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.ejmg.2009.03.013
ER  -