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Article

A case which further refines the critical region for 15q25.2 microduplication phenotypes.

Acta neurologica Belgica - 1 Dec 2016

Monkam Cécile Yossa, Kemeny Stéphan, Miret Anne, Pebrel-Richard Céline, Sarret Catherine

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Share to Abnormalities, Multiple
Share to Chromosomes, Human, Pair 15
Share to Infant, Newborn
Share to Phenotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Segmental Duplications, Genomic

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PMID: 26927603
DOI: 10.1007/s13760-016-0620-7

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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