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Article

Minimal clinical findings in a patient with 15qter microdeletion syndrome: delineation of the associated phenotype.

American journal of medical genetics. Part A - 1 Apr 2012

Jezela-Stanek Aleksandra, Kucharczyk Marzena, Pelc Magdalena, Chrzanowska Krystyna H, Krajewska-Walasek Małgorzata

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Share to Adolescent
Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 15
Share to In Situ Hybridization, Fluorescence

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

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Identifiers

PMID: 22344789
DOI: 10.1002/ajmg.a.34440

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Minimal clinical findings in a patient with 15qter microdeletion syndrome: delineation of the associated phenotype.PMID 22344789Read ↗

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History and molecular characteristics of a patient with terminal deletion of 14q. Is this another syndrome with a striking phenotype?Semantic proximity Read ↗

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