16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2.
Barber JC; Hall V; Maloney VK; Huang S; Roberts AM; Brady AF; Foulds N; Bewes B; Volleth M; Liehr T; Mehnert K; Bateman M; White H; European Journal Of Human Genetics: EJHG, 2013, vol. 21, issue 2, p 182, ISSN 14765438. ISBN 14765438.

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