TY  - GEN
AU  - Inan,Cihan
AU  - Sayin,N Cenk
AU  - Gurkan,Hakan
AU  - Atli,Engin
AU  - Gursoy Erzincan,Selen
AU  - Uzun,Isil
AU  - Sutcu,Havva
AU  - Dogan,Sumeyra
AU  - Ikbal Atli,Emine
AU  - Varol,Fusun
TI  - Schizencephaly accompanied by occipital encephalocele and deletion of chromosome 22q13.32: a case report
SN  - 1551-3823
PY  - 2020///0511
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Agenesis of Corpus Callosum
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 22
KW  - Comparative Genomic Hybridization
KW  - methods
KW  - Encephalocele
KW  - diagnosis
KW  - Female
KW  - Humans
KW  - Schizencephaly
KW  - Young Adult
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1080/15513815.2019.1604921
ER  -