TY  - GEN
AU  - Natera-De Benito,Daniel
AU  - Vidal-Esteban,Arantxa
AU  - Sanchez-Del Pozo,Jaime
AU  - Moreno-Garcia,Marta
AU  - Suela-Rubio,Javier
AU  - Cruz-Rojo,Jaime
AU  - Rivero-Martin,María José
TI  - [Phenotypic variability of the 1q21.1 microdeletion syndrome in members of the same family: relevance of detection of neuropsychiatric disorders for diagnosis of genetic syndromes]
SN  - 1576-6578
PY  - 2016///0922
KW  - Adult
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 1
KW  - genetics
KW  - Comparative Genomic Hybridization
KW  - Disruptive, Impulse Control, and Conduct Disorders
KW  - Female
KW  - Humans
KW  - Hypertelorism
KW  - In Situ Hybridization, Fluorescence
KW  - Intellectual Disability
KW  - Male
KW  - Pedigree
KW  - Penetrance
KW  - Phenotype
KW  - Syndrome
N1  - Publication Type: Case Reports; English Abstract; Journal Article
ER  -