TY  - GEN
AU  - Bijlsma,E K
AU  - Gijsbers,A C J
AU  - Schuurs-Hoeijmakers,J H M
AU  - van Haeringen,A
AU  - Fransen van de Putte,D E
AU  - Anderlid,B-M
AU  - Lundin,J
AU  - Lapunzina,P
AU  - Pérez Jurado,L A
AU  - Delle Chiaie,B
AU  - Loeys,B
AU  - Menten,B
AU  - Oostra,A
AU  - Verhelst,H
AU  - Amor,D J
AU  - Bruno,D L
AU  - van Essen,A J
AU  - Hordijk,R
AU  - Sikkema-Raddatz,B
AU  - Verbruggen,K T
AU  - Jongmans,M C J
AU  - Pfundt,R
AU  - Reeser,H M
AU  - Breuning,M H
AU  - Ruivenkamp,C A L
TI  - Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals
SN  - 1878-0849
PY  - 2009///0901
KW  - Abnormalities, Multiple
KW  - Adolescent
KW  - Adult
KW  - Autistic Disorder
KW  - genetics
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 16
KW  - Comparative Genomic Hybridization
KW  - DNA Mutational Analysis
KW  - Family Health
KW  - Female
KW  - Genetic Testing
KW  - Humans
KW  - Infant
KW  - Intellectual Disability
KW  - Learning Disabilities
KW  - Male
KW  - Speech Disorders
KW  - Young Adult
N1  - Publication Type: Case Reports; Journal Article; Multicenter Study
UR  - https://doi.org/10.1016/j.ejmg.2009.03.006
ER  -