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

Clinical characterization of a girl with trisomy 20q13.2qter and monosomy 13q33.1qter: Delineating phenotype-genotype correlations.

American journal of medical genetics. Part A - 1 Nov 2010

Belar Oihana, Del Pozo Jaime Sanchez, Moreno-García Marta, Cruz-Rojo Jaime, Garin Intza, de Nanclares Guiomar Perez

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 Chromosome Banding
Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 13

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 20

Share to Comparative Genomic Hybridization

Share to Monosomy

Share to Pregnancy

Share to Trisomy

Source

Identifiers

PMID: 20949536
DOI: 10.1002/ajmg.a.33679

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical characterization of a girl with trisomy 20q13.2qter and monosomy 13q33.1qter: Delineating phenotype-genotype correlations.PMID 20949536Read ↗

Trisomy 13 mosaicism in a phenotypically normal child: description of cytogenetic and clinical findings from early pregnancy beyond 2 years of age.Semantic proximity Read ↗

A genotype-first approach for the molecular and clinical characterization of uncommon de novo microdeletion of 20q13.33.Semantic proximity Read ↗

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

Short report: Twins with 20p13 duplication. Case report and comprehensive literature review.Semantic proximity Read ↗

Tetrasomy 21pter-q22.11: molecular, cytogenetic, and clinical findings.Semantic proximity Read ↗

Childhood monosomy 7: epidemiology, biology, and mechanistic implications.Semantic proximity Read ↗

Molecular characterisation of a 3.5 Mb interstitial 14q deletion in a child with several phenotypic anomalies.Semantic proximity Read ↗

Phenotypic Spectrum of Trisomy 18 Mosaicism: a New Patient and Literature Review.Semantic proximity Read ↗

Trisomy 12p and monosomy 4p: phenotype-genotype correlation.Semantic proximity Read ↗

A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review.Semantic proximity Read ↗

Association of 17q24.2-q24.3 deletions with recognizable phenotype and short telomeres.Semantic proximity Read ↗

Refinement of genotype-phenotype correlation in 18 patients carrying a 1q24q25 deletion.Semantic proximity Read ↗

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