Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Monosomy 9pter and trisomy 9q34.11qter in two sisters due to a maternal pericentric inversion

17 Sept 2012

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Genomic variations and chromosomal abnormalities
Share to Genomics and Chromatin Dynamics
Share to Prenatal Screening and Diagnostics

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 22995347
DOI: 10.1016/j.gene.2012.09.018

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Monosomy 9pter and trisomy 9q34.11qter in two sisters due to a maternal pericentric inversionPMID 22995347Read ↗

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

[Subtelomeric deletion 9qter: definition of the syndrome and parental origin in 2 patients].Semantic proximity Read ↗

Trisomy 3q25.1-qter and monosomy 8p23.1-pter in a patient: cytogenetic and molecular analysis with delineation of the phenotype.Semantic proximity Read ↗

Phenotypical variation in cousins with the identical partial trisomy 9 (pter-q22.2) and 7 (q35-qter) at 16 and 23 weeks gestation.Semantic proximity Read ↗

Maternal uniparental isodisomy 11q13qter in a dysmorphic and mentally retarded female with partial trisomy mosaicism 11q13qter.Semantic proximity Read ↗

Clinical and molecular delineation of Tetrasomy 9p syndrome: report of 12 new cases and literature review.Semantic proximity Read ↗

Tetrasomy 9p mosaicism associated with a normal phenotype in two cases.Semantic proximity Read ↗

Unusual Duplication in the Pericentromeric Region of Chromosome 9 in a Patient with Phenotypic Alterations.Semantic proximity Read ↗

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

Tetrasomy 9p due to an intrachromosomal triplication of 9p13-p22.Semantic proximity Read ↗

Three cases of tetrasomy 9p.Semantic proximity Read ↗

Interstitial deletion of 7q31.32 → q33 secondary to a paracentric inversion of a maternal chromosome 7Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.