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

Karyotyping and prenatal diagnosis of 47,XX,+ 8[67]/46,XX [13] Mosaicism: case report and literature review.

BMC medical genomics - 21 Dec 2019

Sun Shaohua, Zhan Fang, Jiang Jiusheng, Zhang Xuerui, Yan Lei, Cai Weiyi, Liu Hailiang, Cao Donghua

Abstract excerpt

BACKGROUND: Trisomy 8 mosaicism has a wide phenotypic variability, ranging from mild dysmorphic features to severe malformations. This report concluded a female pregnant woman with trisomy 8 mosaicism, and carefully cytogenetic diagnoses were performed to give her prenatal diagnostic information. This report also provides more knowledge about trisomy 8 mosaicism and the prenatal diagnostic for clinicians. CASE...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, Pair 8
Share to Karyotyping

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mosaicism

Share to Phenotype

Share to Pregnancy

Share to Prenatal Diagnosis

Share to Trisomy

Share to Uniparental Disomy

Source

Open in PubMed Open full text

Identifiers

PMID: 31864361
DOI: 10.1186/s12920-019-0639-8
PMCID: PMC6925423

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

Karyotyping and prenatal diagnosis of 47,XX,+ 8[67]/46,XX [13] Mosaicism: case report and literature review.PMID 31864361Read ↗

The Karyotype Analysis of Sex Chromosome Mosaicism in Prenatal Diagnosis and Their Clinical OutcomesSemantic proximity Read ↗

Phenotypic Spectrum of Trisomy 18 Mosaicism: a New Patient and Literature Review.Semantic proximity Read ↗

Prenatal diagnosis of mosaic trisomy 8: Clinical report and literature reviewSemantic proximity Read ↗

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

Mosaic Trisomy 9 at Amniocentesis: Prenatal Diagnosis and Molecular Genetic AnalysesSemantic proximity Read ↗

Case report: Detection of fetal trisomy 9 mosaicism by multiple genetic testing methods: Report of two casesSemantic proximity Read ↗

Fetal mosaicism, should conventional karyotype always be performed?Semantic proximity Read ↗

Prenatal diagnosis of 45,X/46,X,dic(X;18) mosaicism: a case reportSemantic proximity Read ↗

Mosaic trisomy 17: variable clinical and cytogenetic presentation.Semantic proximity Read ↗

Chromosomal mosaicism detected by karyotyping and chromosomal microarray analysis in prenatal diagnosisSemantic proximity Read ↗

Prenatal diagnosis of a fetus with trisomy 9 mosaicismSemantic proximity Read ↗

Mosaic trisomy 17 at amniocentesis: Prenatal diagnosis, molecular genetic analysis, and literature reviewSemantic proximity Read ↗

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