TY  - GEN
AU  - Tarlan,Berçin
AU  - Kiratli,Hayyam
AU  - Kılıç,Esra
AU  - Utine,Eda
AU  - Boduroğlu,Koray
TI  - A case of 22q11.2 deletion syndrome with right microphthalmia and left corneal staphyloma
SN  - 1744-5094
PY  - 2015///0420
KW  - Abnormalities, Multiple
KW  - Aphakia
KW  - congenital
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 22
KW  - genetics
KW  - Consanguinity
KW  - Corneal Diseases
KW  - diagnosis
KW  - Developmental Disabilities
KW  - DiGeorge Syndrome
KW  - Growth Disorders
KW  - Heart Septal Defects, Ventricular
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Kidney
KW  - abnormalities
KW  - Magnetic Resonance Imaging
KW  - Male
KW  - Microphthalmos
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.3109/13816810.2013.811269
ER  -