TY  - GEN
AU  - Doornbos,Marianne
AU  - Sikkema-Raddatz,Birgit
AU  - Ruijvenkamp,Claudia A L
AU  - Dijkhuizen,Trijnie
AU  - Bijlsma,Emilia K
AU  - Gijsbers,Antoinet C J
AU  - Hilhorst-Hofstee,Yvonne
AU  - Hordijk,Roel
AU  - Verbruggen,Krijn T
AU  - Kerstjens-Frederikse,W S Mieke
AU  - van Essen,Ton
AU  - Kok,Klaas
AU  - van Silfhout,Anneke T
AU  - Breuning,Martijn
AU  - van Ravenswaaij-Arts,Conny M A
TI  - Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader-Willi critical region, possibly associated with behavioural disturbances
SN  - 1878-0849
PY  - 2009///0901
KW  - Angelman Syndrome
KW  - genetics
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Breakage
KW  - Chromosome Deletion
KW  - Chromosome Disorders
KW  - Chromosomes, Human, Pair 15
KW  - Family Health
KW  - Humans
KW  - Male
KW  - Mental Disorders
KW  - Prader-Willi Syndrome
KW  - Speech Disorders
KW  - Syndrome
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1016/j.ejmg.2009.03.010
ER  -