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

Complete trisomy 10p resulting from an extra stable telocentric chromosome.

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

Lozić Bernarda, Culić Vida, Lasan Ružica, Tomasović Maja, Samija Radenka Kuzmanić, Zemunik Tatijana

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 Banding
Share to Chromosomes, Human, Pair 10
Share to Facies

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

Share to In Situ Hybridization, Fluorescence

Share to Infant, Newborn

Share to Karyotype

Share to Trisomy

Source

Identifiers

PMID: 22628287
DOI: 10.1002/ajmg.a.35384

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 24 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

Complete trisomy 10p resulting from an extra stable telocentric chromosome.PMID 22628287Read ↗

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

10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences.Semantic proximity Read ↗

Consequences of chromosome gain: A new view on trisomy syndromesSemantic proximity Read ↗

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

Double trisomy.Semantic proximity Read ↗

Mouse chromosome 10.Semantic proximity Read ↗

Mouse chromosome 10.Semantic proximity Read ↗

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

Concurrent transposition of distal 6p and 20q to the 22q telomere: a recurrent benign chromosomal variant.Semantic proximity Read ↗

Unbalanced three-way chromosomal translocation leading to deletion 18q and duplication 20pSemantic proximity Read ↗

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

Satellites on the terminal short arm of chromosome 12 (12ps), inherited through several generations in three families: a new variant without phenotypic effect.Semantic proximity Read ↗

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