TY  - GEN
AU  - Kanca,Oguz
AU  - Andrews,Jonathan C
AU  - Lee,Pei-Tseng
AU  - Patel,Chirag
AU  - Braddock,Stephen R
AU  - Slavotinek,Anne M
AU  - Cohen,Julie S
AU  - Gubbels,Cynthia S
AU  - Aldinger,Kimberly A
AU  - Williams,Judy
AU  - Indaram,Maanasa
AU  - Fatemi,Ali
AU  - Yu,Timothy W
AU  - Agrawal,Pankaj B
AU  - Vezina,Gilbert
AU  - Simons,Cas
AU  - Crawford,Joanna
AU  - Lau,C Christopher
AU  - Chung,Wendy K
AU  - Markello,Thomas C
AU  - Dobyns,William B
AU  - Adams,David R
AU  - Gahl,William A
AU  - Wangler,Michael F
AU  - Yamamoto,Shinya
AU  - Bellen,Hugo J
AU  - Malicdan,May Christine V
TI  - De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia
SN  - 1537-6605
PY  - 2020///0316
KW  - Adult
KW  - Amino Acid Sequence
KW  - Animals
KW  - Body Dysmorphic Disorders
KW  - genetics
KW  - Cerebellum
KW  - abnormalities
KW  - Child
KW  - Coloboma
KW  - Developmental Disabilities
KW  - Drosophila melanogaster
KW  - Epilepsy
KW  - Female
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Intellectual Disability
KW  - Male
KW  - Microfilament Proteins
KW  - Mutation
KW  - Nervous System Malformations
KW  - Phenotype
KW  - Sequence Homology
KW  - WD40 Repeats
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.ajhg.2019.06.014
ER  -