15q11.2 microdeletion (BP1–BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: A series of 52 patients

Overview of attention for article published in European Journal of Medical Genetics, January 2015

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Among the highest-scoring outputs from this source (#26 of 1,114)
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15q11.2 microdeletion, developmental delay and congenital heart disease

Questioning Answers, 12 Feb 2015

"Our results support the hypothesis that 15q11.2 (BP1-BP2) microdeletion is associated with developmental delay, abnormal…

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