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Article

Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18

16 Feb 2011

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Share to Genetic Syndromes and Imprinting
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 21326286
DOI: 10.1038/ejhg.2010.252

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Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18PMID 21326286Read ↗

A boy with partial dup(18q)/del(18p) due to a maternal pericentric inversion: Genotype-phenotype correlation and risk of recombinant chromosomes based on systematic review of the literature.Semantic proximity Read ↗

Recurrent proximal 18p monosomy and 18q trisomy in a family due to a pericentric inversion.Semantic proximity Read ↗

Mosaicism of Tetrasomy 18p: Clinical and Cytogenetic Findings in a Female Child.Semantic proximity Read ↗

Isochromosome 18p Results from Maternal Meiosis II NondisjunctionSemantic proximity Read ↗

Prenatal genetic diagnosis in a fetus with tetrasomy 18p from maternal trisomy 18p: a case reportSemantic proximity Read ↗

Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18.Semantic proximity Read ↗

Atypical 18p- syndrome associated with partial trisomy 16p in a chromosomally unbalanced child of consanguineous parents with an identical balanced translocationSemantic proximity Read ↗

Monosomy 9pter and trisomy 9q34.11qter in two sisters due to a maternal pericentric inversionSemantic proximity Read ↗

Monosomy 19pter and trisomy 19q13-qter in two siblings arising from a maternal pericentric inversion: Clinical data and molecular characterizationSemantic proximity Read ↗

[Phenotypic and genetic analysis of a child featuring multiple malformations due to chromosome 18p deletion].Semantic proximity Read ↗

Clinical and molecular characterization of individuals with 18p deletion: a genotype-phenotype correlation.Semantic proximity Read ↗

Interstitial deletion of 11q in a mother and fetus: implications of directly transmitted chromosomal imbalances for prenatal genetic counselingSemantic proximity Read ↗

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