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

[Prenatal diagnosis of a fetus with two small supernumerary marker chromosomes].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics - 10 Dec 2019

Zhang Jian, Jiang Yu, Cai Meijiao, Ge Yunsheng, Zhou Yulin, Wang Wenbo

Abstract excerpt

OBJECTIVE: To explore the clinical significance of a prenatal case with two small supernumerary marker chromosomes (sSMC) through identification of their origins. METHODS: G-banding chromosomal karyotyping analysis were carried out on fetal amniotic fluid sample and peripheral blood samples from both patients. Fluorescence in situ hybridization (FISH) and single nucleotide polymorphism-array (SNP-array) were used...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Aberrations
Share to Chromosome Banding

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to In Situ Hybridization, Fluorescence

Share to Karyotyping

Share to Polymorphism, Single Nucleotide

Share to Pregnancy

Share to Prenatal Diagnosis

Source

Identifiers

PMID: 31813153
DOI: 10.3760/cma.j.issn.1003-9406.2019.12.018

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Prenatal diagnosis of a fetus with two small supernumerary marker chromosomes].PMID 31813153Read ↗

[Prenatal diagnosis of three fetuses with small supernumerary marker chromosomes].Semantic proximity Read ↗

[Study of two cases of prenatally detected small supernumerary marker chromosomes].Semantic proximity Read ↗

[Prenatal diagnosis of two fetuses with de novo small supernumerary markers by single nucleotide polymorphism array based comparative genomic hybridization].Semantic proximity Read ↗

[SNP-chip technology for identification of origins for prenatally detected marker chromosomes].Semantic proximity Read ↗

[Detection of small supernumerary marker chromosome by single nucleotide polymorphism microarray chips].Semantic proximity Read ↗

Retrospectively investigating the 12-year experience of prenatal diagnosis of small supernumerary marker chromosomes through array comparative genomic hybridizationSemantic proximity Read ↗

Prenatal diagnosis and molecular cytogenetic identification of small supernumerary marker chromosomes: analysis of three prenatal cases using chromosome microarray analysis.Semantic proximity Read ↗

[Prenatal diagnosis of a Pallister-Killian syndrome case through analysis of a supernumerary chromosome using single nucleotide polymorphism array].Semantic proximity Read ↗

Molecular Delineation of De Novo Small Supernumerary Marker Chromosomes in Prenatal Diagnosis, A Retrospective StudySemantic proximity Read ↗

Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.Semantic proximity Read ↗

Handling small supernumerary marker chromosomes in prenatal diagnosticsSemantic proximity Read ↗

Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1-q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality.Semantic proximity Read ↗

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