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

Distal trisomy 10q syndrome: phenotypic features in a child with inverted duplicated 10q25.1-q26.3.

Clinical dysmorphology - 1 Jul 2010

Carter Melissa T, Dyack Sarah, Richer Julie

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 Chromosome Aberrations
Share to Chromosome Inversion
Share to Chromosomes, Human, Pair 10

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

Share to Gene Duplication

Share to Pregnancy

Share to Syndrome

Share to Trisomy

Source

Identifiers

PMID: 20354439
DOI: 10.1097/MCD.0b013e3283377915

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 Oct 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

Distal trisomy 10q syndrome: phenotypic features in a child with inverted duplicated 10q25.1-q26.3.PMID 20354439Read ↗

10p monosomy, a phenotypic variant.Semantic proximity Read ↗

Terminal deletion of chromosome 10q: clinical features and literature review.Semantic proximity Read ↗

Partial trisomy 10q with mild phenotype caused by an unbalanced X;10 translocation.Semantic proximity Read ↗

A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11 --> q223?Semantic proximity Read ↗

Deletion of the distal long arm of chromosome 10; is there a characteristic phenotype? A report of 15 de novo and familial cases.Semantic proximity Read ↗

Molecular cytogenetics and phenotype characterization of a de novo pure partial trisomy 10(q24.33-qter).Semantic proximity Read ↗

A Patient with Trisomy 4p and Monosomy 10qSemantic proximity Read ↗

Characterization of 10p Deletions Suggests Two Nonoverlapping Regions Contribute to the DiGeorge Syndrome PhenotypeSemantic proximity Read ↗

Hearing loss, coloboma and left ventricular enlargement in a boy with an interstitial 10q26 deletion.Semantic proximity Read ↗

A new case of proximal 10q partial trisomy.Semantic proximity Read ↗

Molecular cytogenetic analysis of a de novo interstitial deletion of chromosome 10q (q25.3q26.13) in a male child with ambiguous genitalia: Evidence for a new critical region for genital development.Semantic proximity Read ↗

Chromosome 10q26 deletion syndrome: Two new cases and a review of the literature.Semantic proximity Read ↗

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