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

Transmitted duplication of 12q21.32-12q22 includes 48 genes and has no apparent phenotypic consequences.

American journal of medical genetics. Part A - 15 Mar 2007

Barber John C K, Maloney Viv K, Kirchhoff Maria, Thomas N Simon, Boyle Tracy A, Castle Bruce

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 Disorders
Share to Chromosomes, Human, Pair 12
Share to Family Health

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Duplication

Share to In Situ Hybridization, Fluorescence

Share to Karyotyping

Share to Nucleic Acid Hybridization

Source

Identifiers

PMID: 17318843
DOI: 10.1002/ajmg.a.31614

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

Transmitted duplication of 12q21.32-12q22 includes 48 genes and has no apparent phenotypic consequences.PMID 17318843Read ↗

Deletion 22q11: Spectrum of Associated DisordersSemantic proximity Read ↗

Review of the Pathophysiology and Clinical Manifestations of 22q11.2 Deletion and Duplication SyndromesSemantic proximity Read ↗

A family with a 1.17 Mb deletion of 12q12: refining genotype-phenotype correlation.Semantic proximity Read ↗

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

A transmitted deletion of 2q13 to 2q14.1 causes no phenotypic abnormalities.Semantic proximity Read ↗

Partial duplication of the long arm of chromosome 22 (22q 13) with complete 22 trisomy phenotype.Semantic proximity Read ↗

Duplication of 18q21.32-q22.3 identified in a stillborn and two relatives with minimal dysmorphic features.Semantic proximity Read ↗

Pure familial 6q21q22.1 duplication in two generationsSemantic proximity Read ↗

Duplication (22)(q11.22-q11.23) without coloboma and cleft lip or palate.Semantic proximity Read ↗

Our evolving understanding of 22q.11 deletion syndrome.Semantic proximity Read ↗

Phenotype variant of the common duplication at 17p11.2.Semantic proximity Read ↗

Clinical utility gene card for: 16p13.11 microdeletion syndrome.Semantic proximity Read ↗

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