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Am J Med Genet A. 2013 Jun;161A(6):1501-4. doi: 10.1002/ajmg.a.35912. Epub 2013 Apr 30.

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

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  • 1Department of Medical Genetics, Medical University of Silesia, Sosnowiec, Poland. mary.kow@interia.pl
PMID:
23633153
[PubMed - in process]
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