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

[Genetic analysis of a supernumerary derivative chromosome 15].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics - 1 Feb 2012

Wang Fang, Yang Yao, Wang Chun-zhi, He X-iyu

Abstract excerpt

OBJECTIVE: To detect and analyze a supernumerary derivative chromosome 15 with combined cytogenetic and molecular techniques, and to discuss the correlation between genomic copy number variations (CNVs) and clinical phenotypes. METHODS: G-banded chromosome analysis and multiplex ligation-dependent probe amplification (MLPA) were carried out. The whole genome of the patient was also analyzed with array-comparative...

Read the complete abstract on PubMed

Topics

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

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

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

Share to Cytogenetic Analysis

Share to DNA Copy Number Variations

Share to Phenotype

Source

Identifiers

PMID: 22311498
DOI: 10.3760/cma.j.issn.1003-9406.2012.01.019

Provenance

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

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Genetic analysis of a supernumerary derivative chromosome 15].PMID 22311498Read ↗

[Molecular cytogenetic study of a case with ring chromosome 15].Semantic proximity Read ↗

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

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

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

[Phenotypic and genetic characteristics of a child with 7p15 deletion syndrome].Semantic proximity Read ↗

Chromosome 15q11-q13 Duplication Syndrome: A Review of the Literature and 14 New Cases.Semantic proximity Read ↗

Autistic disorder phenotype associated to a complex 15q intrachromosomal rearrangement.Semantic proximity Read ↗

[Clinical phenotype and genetic analysis of a patient with a heterozygous 6p25.3 deletion and partial trisomy 15q].Semantic proximity Read ↗

Unraveling the genomic architecture of supernumerary (iso-) dicentric chromosomes in Dup15q syndrome: Insight from a systematic literature-based studySemantic proximity Read ↗

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

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

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

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