Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes.
Rosenfeld JA; Traylor RN; Schaefer GB; McPherson EW; Ballif BC; Klopocki E; Mundlos S; Shaffer LG; Aylsworth AS; European Journal Of Human Genetics: EJHG, 2012, vol. 20, issue 7, p 754, ISSN 14765438. ISBN 14765438.

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