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15q11.2 microdeletion - seven new patients with delayed development and/or behavioural problems.

C von der Lippe1, C Rustad, K Heimdal

  • 1Dep. of Medical Genetics, Oslo University Hospital, Oslo, Norway. Charlotte.Von.Der.Lippe2@oslo-universitetssykehus.no

European Journal of Medical Genetics
|December 29, 2010
PubMed
Summary

The 15q11.2 microdeletion syndrome, affecting four genes, is confirmed in seven new patients. This genetic condition is linked to learning difficulties and developmental delays, often inherited from mildly affected parents.

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