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

Inheritance of balanced translocation t(17; 22) from a Down syndrome mother to a phenotypically normal daughter.

Genetics and molecular research : GMR - 28 Aug 2015

Liu X Y, Jiang Y T, Wang R X, Luo L L, Liu Y H, Liu R Z

Abstract excerpt

We report that a 30-year-old woman with mental retardation was referred for prenatal diagnoses during pregnancy. An ultrasound scan showed that the heart structure and function of the fetus were normal. Cytogenetic analysis showed that the female karyotype was 47,XX, t(17; 22) (q21; q11), +21. The woman's husband had a normal male karyotype and was phenotypically normal. During this first pregnancy, an...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Amniotic Fluid
Share to Chromosome Banding
Share to Chromosomes, Human, Pair 17

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

Share to Chromosomes, Human, Pair 22

Share to Down Syndrome

Share to Inheritance Patterns

Share to Mothers

Share to Nuclear Family

Source

Identifiers

PMID: 26345964
DOI: 10.4238/2015.August.28.11

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

Inheritance of balanced translocation t(17; 22) from a Down syndrome mother to a phenotypically normal daughter.PMID 26345964Read ↗

Familial transmission of a deletion of chromosome 21 derived from a translocation between chromosome 21 and an inverted chromosome 22.Semantic proximity Read ↗

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

Unusual chromosomal mosaicism as a cause of mental retardation and congenital malformations in a familial reciprocal translocation carrier, t(17;22)(q24.2;q11.23)Semantic proximity Read ↗

Ultrasonographic findings and prenatal diagnosis of complete trisomy 17p syndrome: A case report and review of the literature.Semantic proximity Read ↗

20 p duplication as a result of parental translocation: familial case report and a contribution to the clinical delineation of the syndrome.Semantic proximity Read ↗

Clinical, cytogenetic, and molecular evaluation of a patient with partial trisomy 21 (21q11-q22) lacking the classical Down syndrome phenotype.Semantic proximity Read ↗

Partial trisomy of chromosome 21 without the Down syndrome phenotype.Semantic proximity Read ↗

A case of apparent trisomy 21 without the Down's syndrome phenotype.Semantic proximity Read ↗

Prenatal diagnosis of familial ring 21 chromosomeSemantic proximity Read ↗

Recombinant Down syndrome: a case report and literature review.Semantic proximity Read ↗

A prenatal diagnosis case of partial duplication 21q21.1-q21.2 with normal phenotype maternally inherited.Semantic proximity Read ↗

Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.Semantic proximity Read ↗

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