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Article

De novo 13q31.1-q32.1 interstitial deletion encompassing the miR-17-92 cluster in a patient with Feingold syndrome-2.

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

Tassano E, Di Rocco M, Signa S, Gimelli G

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Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 13
Share to Comparative Genomic Hybridization
Share to Eyelids

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Intellectual Disability

Share to Limb Deformities, Congenital

Share to Microcephaly

Share to RNA, Long Noncoding

Source

Identifiers

PMID: 23495052
DOI: 10.1002/ajmg.a.35781

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

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De novo 13q31.1-q32.1 interstitial deletion encompassing the miR-17-92 cluster in a patient with Feingold syndrome-2.PMID 23495052Read ↗

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