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Article

A familial deletion of 16q21 characterized by an SNP array and associated with a normal phenotype.

American journal of medical genetics. Part A - 1 Jun 2013

Kowalczyk Malgorzata, Tomaszewska Agnieszka, Podbiol-Palenta Agnieszka, Remiszewska Barbara, Galjaard Robert Jan H, Zajaczek Stanislaw, Srebniak Malgorzata I

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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PMID: 23633153
DOI: 10.1002/ajmg.a.35912

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