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Article

Unusual features in children with inv dup(15) supernumerary marker: a study of genotype-phenotype correlation in Taiwan.

European journal of pediatrics - 1 Feb 1998

Hou J W, Wang T R

Abstract excerpt

UNLABELLED: Recent molecular cytogenetic studies have elucidated the origin and nature of extra structurally abnormal chromosomes (ESACs) or small supernumerary chromosomes, which are often associated with developmental delay and malformations. We studied the prevalence of inv dup(15) in a nationwide screening programme for mentally retarded children in Taiwan and tried to correlate the genotype and phenotype in...

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Source

Identifiers

PMID: 9504785
DOI: 10.1007/s004310050782

Genes

GABRB3

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Unusual features in children with inv dup(15) supernumerary marker: a study of genotype-phenotype correlation in Taiwan.PMID 9504785Read ↗

The inv dup (15) or idic (15) syndrome (Tetrasomy 15q)Semantic proximity Read ↗

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 ↗

Partial hexasomy of chromosome 15.Semantic proximity Read ↗

Cytogenetic and molecular characterization of inverted duplicated chromosomes 15 from 11 patients.Semantic proximity Read ↗

A case of mosaic supernumerary ring chromosome 15 with two copies of the segment 15p11.1-q14.Semantic proximity Read ↗

De novo interstitial duplication of the 15q11.2-q14 PWS/AS region of maternal origin: Clinical description, array CGH analysis, and review of the literature.Semantic proximity Read ↗

Rare partial trisomy and tetrasomy of 15q11-q13 associated with developmental delay and autism spectrum disorderSemantic proximity Read ↗

Phenotypic spectrum of 20 novel patients with molecularly defined supernumerary marker chromosomes 15 and a review of the literature.Semantic proximity Read ↗

[Analysis of 10 patients with duplications of 15q11q13 region and autism features].Semantic proximity Read ↗

Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.Semantic proximity Read ↗

Expanding deep phenotypic spectrum associated with atypical pathogenic structural variations overlapping 15q11-q13 imprinting region.Semantic proximity Read ↗

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