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Article

Incidental finding of paternal UPD15 in a child with a deletion of 11q21-q22.3, presenting with developmental delay, coloboma and characteristic dysmorphic features.

Clinical dysmorphology - 1 Apr 2016

Tucker Tracy, Steinraths Michelle, Oh Tracey, Nelson Tanya N, Van Allen Margot I, Brown Lindsay, Schlade-Bartusiak Kamilla

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Share to Chromosomes, Human, Pair 11
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 26636500
DOI: 10.1097/MCD.0000000000000108

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