TY  - GEN
AU  - Chowdhury,Shimul
AU  - Bandholz,Anne M
AU  - Parkash,Sandhya
AU  - Dyack,Sarah
AU  - Rideout,Andrea L
AU  - Leppig,Kathleen A
AU  - Thiese,Heidi
AU  - Wheeler,Patricia G
AU  - Tsang,Marilyn
AU  - Ballif,Blake C
AU  - Shaffer,Lisa G
AU  - Torchia,Beth S
AU  - Ellison,Jay W
AU  - Rosenfeld,Jill A
TI  - Phenotypic and molecular characterization of 19q12q13.1 deletions: a report of five patients
SN  - 1552-4833
PY  - 2015///0413
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Adolescent
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 19
KW  - Comparative Genomic Hybridization
KW  - Facies
KW  - Female
KW  - Genetic Diseases, Inborn
KW  - diagnosis
KW  - Humans
KW  - Infant
KW  - Male
KW  - Phenotype
KW  - Syndrome
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1002/ajmg.a.36201
ER  -