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 patient with a duplication of chromosome 3p (p24.1p26.2): a comparison with other partial 3p trisomies.

American journal of medical genetics. Part A - 1 Feb 2014

Natera-de Benito Daniel, García-Pérez M Asunción, Martínez-Granero Miguel Ángel, Izquierdo-López Luis

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 Chromosome Duplication
Share to Chromosomes, Human, Pair 3
Share to Facies

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

Share to Phenotype

Share to Trisomy

Source

Identifiers

PMID: 24311452
DOI: 10.1002/ajmg.a.36164

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 17 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

A patient with a duplication of chromosome 3p (p24.1p26.2): a comparison with other partial 3p trisomies.PMID 24311452Read ↗

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 ↗

A report of a new case of an interstitial deletion at 3p25.3 and expansion of the clinical phenotype.Semantic proximity Read ↗

Partial trisomy 9p12p21.3 with a normal phenotype.Semantic proximity Read ↗

A patient with a de-novo deletion 3p25.3 and features overlapping with Rubinstein-Taybi syndrome.Semantic proximity Read ↗

Partial distal trisomy 3p. A partial autosomal trisomy without major dysmorphic features.Semantic proximity Read ↗

De novo direct duplication 3 (p25-->pter): a previously undescribed chromosomal aberration.Semantic proximity Read ↗

Partial 3q duplication syndrome and assignment of D3S5 to 3q25-3q28.Semantic proximity Read ↗

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

A boy with partial trisomy of chromosome 3q24-q28 from paternal balanced insertion and multiple congenital anomalies.Semantic proximity Read ↗

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

3q29 microduplication syndrome: Description of two new cases and delineation of the minimal critical regionSemantic proximity Read ↗

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

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