TY  - GEN
AU  - Snijders Blok,Charlotte
AU  - Corsten-Janssen,Nicole
AU  - FitzPatrick,David R
AU  - Romano,Corrado
AU  - Fichera,Marco
AU  - Vitello,Girolamo Aurelio
AU  - Willemsen,Marjolein H
AU  - Schoots,Jeroen
AU  - Pfundt,Rolph
AU  - van Ravenswaaij-Arts,Conny M A
AU  - Hoefsloot,Lies
AU  - Kleefstra,Tjitske
TI  - Definition of 5q11.2 microdeletion syndrome reveals overlap with CHARGE syndrome and 22q11 deletion syndrome phenotypes
SN  - 1552-4833
PY  - 2016///0516
KW  - 22q11 Deletion Syndrome
KW  - diagnosis
KW  - Adolescent
KW  - Adult
KW  - CHARGE Syndrome
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosome Disorders
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 5
KW  - Comparative Genomic Hybridization
KW  - Diagnosis, Differential
KW  - Facies
KW  - Female
KW  - Genetic Association Studies
KW  - Humans
KW  - Infant
KW  - Male
KW  - Phenotype
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/ajmg.a.36680
ER  -