TY  - GEN
AU  - Schirwani,Schaida
AU  - Smith,Kath
AU  - Balasubramanian,Meena
TI  - Clinical and molecular characterization of the first familial report of 1p32 microdeletion
SN  - 1473-5717
PY  - 2018///0903
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Adult
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 1
KW  - Comparative Genomic Hybridization
KW  - DNA-Binding Proteins
KW  - Developmental Disabilities
KW  - Female
KW  - Humans
KW  - LDL-Receptor Related Proteins
KW  - Male
KW  - Microcephaly
KW  - Pedigree
KW  - Phenotype
KW  - Transcription Factors
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1097/MCD.0000000000000209
ER  -