TY  - GEN
AU  - Şimşek-Kiper,Pelin Özlem
AU  - Bayram,Yavuz
AU  - Ütine,Gülen Eda
AU  - Alanay,Yasemin
AU  - Boduroğlu,Koray
TI  - A de novo 11q23 deletion in a patient presenting with severe ophthalmologic findings, psychomotor retardation and facial dysmorphism
SN  - 2791-6421
PY  - 2015///0922
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Child, Preschool
KW  - Craniofacial Abnormalities
KW  - Face
KW  - abnormalities
KW  - Facies
KW  - Female
KW  - Humans
KW  - Jacobsen Distal 11q Deletion Syndrome
KW  - Muscular Atrophy
KW  - Ophthalmoplegia
KW  - Psychomotor Disorders
N1  - Publication Type: Case Reports; Journal Article
ER  -