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

A case of 9q21.11q22.1 triplication with novel ophthalmic features.

Clinical dysmorphology - 1 Jan 2017

Vallabh Neeru A, Buchanan Aram, Ainscough Magda, Newman William, Fryer Alan

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 Child, Preschool
Share to Chromosomes, Human, Pair 11
Share to Chromosomes, Human, Pair 9
Share to Eye Abnormalities

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to In Situ Hybridization, Fluorescence

Share to Oligonucleotide Array Sequence Analysis

Share to Phenotype

Share to Trisomy

Source

Identifiers

PMID: 27749393
DOI: 10.1097/MCD.0000000000000157

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

A case of 9q21.11q22.1 triplication with novel ophthalmic features.PMID 27749393Read ↗

Nonrecurrent Triplication of 5q21.3q23.3: A Case Report and Review of the Literature.Semantic proximity Read ↗

A novel presentation of a rare chromosome 21q22.2 deletion.Semantic proximity Read ↗

Complete Trisomy 9 with unusual phenotypic associations.Semantic proximity Read ↗

Ocular manifestations of trisomy 8 mosaicim: a rare case report.Semantic proximity Read ↗

Triplication of 16p12.1p12.3 associated with developmental and growth delay and distinctive facial features.Semantic proximity Read ↗

A familial inverted duplication/deletion of 2p25.1–25.3 provides new clues on the genesis of inverted duplicationsSemantic proximity Read ↗

4.3‐Mb triplication of 4q32.1–q32.2: Report of a family through two generationsSemantic proximity Read ↗

Intrachromosomal partial triplication of chromosome 13 secondary to a paternal duplication with mild phenotypic effect.Semantic proximity Read ↗

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

8p23 duplication reconsidered: is it a true euchromatic variant with no clinical manifestation?Semantic proximity Read ↗

Parental origin and mechanisms of formation of triploidy: a study of 25 casesSemantic proximity Read ↗

Gonadoblastoma in a patient with del(9)(p22) and sex reversalSemantic proximity Read ↗

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