Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader-Willi critical region, possibly associated with behavioural disturbances.

Doornbos, Marianne

Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader-Willi critical region, possibly associated with behavioural disturbances. [electronic resource] - European journal of medical genetics - 108-15 p. digital

Publication Type: Case Reports; Journal Article

1878-0849

10.1016/j.ejmg.2009.03.010 doi


Angelman Syndrome--genetics
Child
Child, Preschool
Chromosome Breakage
Chromosome Deletion
Chromosome Disorders--genetics
Chromosomes, Human, Pair 15
Family Health
Humans
Male
Mental Disorders--genetics
Prader-Willi Syndrome--genetics
Speech Disorders
Syndrome