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 girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review.

Clinical dysmorphology - 1 Jul 2016

Pavone Piero, Praticò Andrea D, Falsaperla Raffaele, Ruggieri Martino, Neri Giovanni, Pavone Vito, Zollino Marcella

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

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

Share to Comparative Genomic Hybridization

Share to Facies

Share to In Situ Hybridization, Fluorescence

Share to Syndrome

Source

Identifiers

PMID: 26918294
DOI: 10.1097/MCD.0000000000000119

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 18 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 girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review.PMID 26918294Read ↗

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

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

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

Case Report: A Case Report and Literature Review of 3p Deletion SyndromeSemantic proximity Read ↗

Phenotypes of 8q13.2-q13.3 microdeletion: Case report and literature review of an emerging recurrent microdeletion syndrome.Semantic proximity Read ↗

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

Molecular characterization of a patient with 3p deletion syndrome and a review of the literature.Semantic proximity Read ↗

A clinical case report and literature review of the 3q29 microdeletion syndromeSemantic proximity Read ↗

[Phenotypic and genetic analysis of a child with multiple malformations due to 10p13p15.3 duplication].Semantic proximity Read ↗

9p13.1p13.3 interstitial deletion: A case report and further delineation of a rare condition.Semantic proximity Read ↗

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

Karyotype-phenotype analysis and molecular delineation of a 3p26 deletion/8q24.3 duplication case with a virtually normal phenotype and mild cognitive deficit.Semantic proximity Read ↗

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