TY  - GEN
AU  - Cohen,J S
AU  - Srivastava,S
AU  - Farwell Hagman,K D
AU  - Shinde,D N
AU  - Huether,R
AU  - Darcy,D
AU  - Wallerstein,R
AU  - Houge,G
AU  - Berland,S
AU  - Monaghan,K G
AU  - Poretti,A
AU  - Wilson,A L
AU  - Chung,W K
AU  - Fatemi,A
TI  - Further evidence that de novo missense and truncating variants in ZBTB18 cause intellectual disability with variable features
SN  - 1399-0004
PY  - 2017///0602
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Adult
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 1
KW  - Exome
KW  - Female
KW  - Haploinsufficiency
KW  - Humans
KW  - Intellectual Disability
KW  - Magnetic Resonance Imaging
KW  - Male
KW  - Microcephaly
KW  - Mutation
KW  - Mutation, Missense
KW  - Pregnancy
KW  - Repressor Proteins
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1111/cge.12861
ER  -