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Article

Inv dup(15) supernumerary marker chromosomes.

Journal of medical genetics - 1 Aug 1994

Webb T

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Share to Aneuploidy
Share to Chromosome Disorders
Share to Chromosome Inversion
Share to Chromosomes, Human, Pair 15

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fetal Diseases

Share to Genomic Imprinting

Share to Mosaicism

Share to Prader-Willi Syndrome

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Identifiers

PMID: 7815414
DOI: 10.1136/jmg.31.8.585
PMCID: PMC1050018

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Uniparental disomy (UPD) other than 15: phenotypes and bibliography updated.Semantic proximity Read ↗

New euchromatic variant dup(11)(p15.3p15.1) transmitted through two generations defined by low coverage whole genome sequencing.Semantic proximity Read ↗

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Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexity.Semantic proximity Read ↗

Inv dup(15): contribution to the clinical definition of phenotype.Semantic proximity Read ↗

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