TY  - GEN
AU  - Gerkes,Erica H
AU  - Hordijk,Roel
AU  - Dijkhuizen,Trijnie
AU  - Sival,Deborah A
AU  - Meiners,Linda C
AU  - Sikkema-Raddatz,Birgit
AU  - van Ravenswaaij-Arts,Conny M A
TI  - Bilateral polymicrogyria as the indicative feature in a child with a 22q11.2 deletion
SN  - 1878-0849
PY  - 2011///0111
KW  - Cerebral Cortex
KW  - abnormalities
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 22
KW  - Developmental Disabilities
KW  - genetics
KW  - DiGeorge Syndrome
KW  - Humans
KW  - Infant
KW  - Intellectual Disability
KW  - Magnetic Resonance Imaging
KW  - Male
KW  - Malformations of Cortical Development
KW  - Microcephaly
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1016/j.ejmg.2010.05.003
ER  -