TY  - GEN
AU  - Koolen,David A
AU  - Reardon,William
AU  - Rosser,Elisabeth M
AU  - Lacombe,Didier
AU  - Hurst,Jane A
AU  - Law,Caroline J
AU  - Bongers,Ernie M H F
AU  - van Ravenswaaij-Arts,Conny M
AU  - Leisink,Martijn A R
AU  - van Kessel,Ad Geurts
AU  - Veltman,Joris A
AU  - de Vries,Bert B A
TI  - Molecular characterisation of patients with subtelomeric 22q abnormalities using chromosome specific array-based comparative genomic hybridisation
SN  - 1018-4813
PY  - 2005///1027
KW  - Adolescent
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 22
KW  - genetics
KW  - Female
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Infant
KW  - Intellectual Disability
KW  - Karyotyping
KW  - Language Development Disorders
KW  - Male
KW  - Molecular Biology
KW  - Muscle Hypotonia
KW  - Nucleic Acid Hybridization
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/sj.ejhg.5201456
ER  -