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

[Partial trisomy 3, 22: 47, XX, +der (22) t (3; 22) (q29; q11,1) mat.: report of a case].

Anales espanoles de pediatria - 1 Nov 1990

Paredes Cencillo C, Mir Plana M, Sequi Canet J M, Montagud E, Gregori Romero M, López Ginés C, Gil R

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 Chromosomes, Human, Pair 22
Share to Cytogenetics
Share to Infant
Share to Infant, Newborn

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

Share to Intellectual Disability

Share to Pedigree

Share to Translocation, Genetic

Share to Trisomy

Source

Identifiers

PMID: 2096769

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 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

[Partial trisomy 3, 22: 47, XX, +der (22) t (3; 22) (q29; q11,1) mat.: report of a case].PMID 2096769Read ↗

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

[Trisomy 8 mosaicism: 46,XX/47,XX+8].Semantic proximity Read ↗

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

Partial duplication of the long arm of chromosome 22 (22q 13) with complete 22 trisomy phenotype.Semantic proximity Read ↗

Partial trisomy 13q: report of a case.Semantic proximity Read ↗

[5 cases of structural anomalies of the X chromosome and a case of 45,X,2(p+q-)].Semantic proximity Read ↗

Partial trisomy (11;22) syndrome with manifestations of Goldenhar sequence due to maternal balanced t(11;22).Semantic proximity Read ↗

Disorder of sex development in an infant with molecularly confirmed 46,XY, +der(10)t(10;21)(q21.1;q21.3), -21.Semantic proximity Read ↗

[Partial trisomy 1q due to maternal translocation].Semantic proximity Read ↗

Phenotype of a patient with pure partial trisomy 2p(p23-->pter).Semantic proximity Read ↗

DOUBLE TRISOMY MOSAICISM 48,XXX,+8/46,XX IN A FEMALE: THE FIRST REPORTED CASE.Semantic proximity Read ↗

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

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