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

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

American journal of medical genetics. Part A - 1 Jul 2012

Henson Kaylee E, Hines Karrie A, Weaver David D, Torres Wilfredo M, Verbrugge Jennifer, Stone Kristyne, Vance Gail H

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 Abnormalities, Multiple
Share to Child, Preschool
Share to Chromosomes, Human, Pair 18

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Family

Share to Genetic Association Studies

Share to Stillbirth

Share to Trisomy

Share to Young Adult

Source

Identifiers

PMID: 22653737
DOI: 10.1002/ajmg.a.35405

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Duplication of 18q21.32-q22.3 identified in a stillborn and two relatives with minimal dysmorphic features.PMID 22653737Read ↗

Duplication 18q21.31-q22.2.Semantic proximity Read ↗

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

A case of de novo mosaic 18q21.3 deletion with a mild phenotype.Semantic proximity Read ↗

50 Years Ago in TheJournalofPediatrics: An Update on the Phenotypic Map of 18q Deletions.Semantic proximity Read ↗

Duplication of the Williams-Beuren critical region: case report and further delineation of the phenotypic spectrum.Semantic proximity Read ↗

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

Prenatal and Postnatal Diagnosis and Phenotype of 8p23.2p22 Duplication in One FamilySemantic proximity Read ↗

Prenatal diagnosis of familial submicroscopic duplication at 18q22.3 without phenotypic abnormalities.Semantic proximity Read ↗

Expanding the phenotype of 22q13.3 deletion: report of a case detected prenatally.Semantic proximity Read ↗

A novel 5p15.33-14.1 deletion and 4q34.24-35.2 duplication in a patient with mental retardation, dysmorphic features and severe speech delay.Semantic proximity Read ↗

8p23.2p22 deletion: a case report of a large deletion encompassing 8p23.1 with additional clinical features.Semantic proximity Read ↗

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

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