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Article

Interstitial deletion 14q31.1q31.3 transmitted from a mother to her daughter, both with features of hemifacial microsomia.

Journal of applied genetics - 1 Aug 2013

Gimelli S, Cuoco C, Ronchetto P, Gimelli G, Tassano E

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Share to Chromosome Banding
Share to Chromosomes, Human, Pair 14
Share to Comparative Genomic Hybridization
Share to Ear

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Facial Asymmetry

Share to Goldenhar Syndrome

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PMID: 23645319
DOI: 10.1007/s13353-013-0150-4

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Interstitial deletion 14q31.1q31.3 transmitted from a mother to her daughter, both with features of hemifacial microsomia.PMID 23645319Read ↗

Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndromeSemantic proximity Read ↗

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A novel microdeletion involving the 13q31.3-q32.1 region in a patient with normal intelligence.Semantic proximity Read ↗

A de novo 1.38 Mb duplication of 1q31.1 in a boy with hemifacial microsomia, anophthalmia, anotia, macrostomia, and cleft lip and palate.Semantic proximity Read ↗

9p13.1p13.3 interstitial deletion: A case report and further delineation of a rare condition.Semantic proximity Read ↗

Whole-exome sequencing for monozygotic twins discordant for hemifacial microsomia.Semantic proximity Read ↗

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

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Functional Genomics via Zebrafish CRISPR Reveals Pathogenic Landscape of 16 Candidate Genes in Hemifacial MicrosomiaSemantic proximity Read ↗

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