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

Karyotype analysis of amniotic fluid cells and report of chromosomal abnormalities in 15,401 cases of Iranian women

30 Sept 2021

Abstract excerpt

The aim of present study was to assess the karyotypes of amniotic fluid cells and find the frequency of chromosomal abnormalities and their significance in clinical setting. A total of 15,401 pregnant women were assessed from March 2016 to May 2019, and 14,968 amniotic fluid samples were successfully cultured. These fetuses were grouped according to different indications including advanced maternal age, abnormal...

Read the complete abstract on PubMed

Topics

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

Share to Congenital Anomalies and Fetal Surgery
Share to Parvovirus B19 Infection Studies
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 34593920
DOI: 10.1038/s41598-021-98928-3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Karyotype analysis of amniotic fluid cells and report of chromosomal abnormalities in 15,401 cases of Iranian womenPMID 34593920Read ↗

Prenatal diagnosis of fetal chromosomal abnormalities among 2318 pregnant women with indications in southern China: a retrospective studySemantic proximity Read ↗

Incidence and Spectrum of Chromosome Abnormalities in Miscarriage Samples: A Retrospective Study of 330 CasesSemantic proximity Read ↗

Comparison of chromosomal microarray and karyotyping in prenatal diagnosis using 491 amniotic fluid samplesSemantic proximity Read ↗

Prenatal diagnosis and counseling of fetal chromosomes with structural abnormalitiesSemantic proximity Read ↗

Clinical and Cytogenetic Findings on 31,615 Mid-trimester AmniocentesesSemantic proximity Read ↗

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

Rare structural chromosomal abnormalities in prenatal diagnosis; clinical and cytogenetic findings on 10125 prenatal cases.Semantic proximity Read ↗

[Frequency of prevalence of Turner syndrome in fetuses of patients referred to genetic amniocentesis in 2007-2011].Semantic proximity Read ↗

Application of Chromosomal Karyotype Analysis Combined With Chromosomal Microarray Analysis in the Amniotic Fluid of Advanced Maternal AgeSemantic proximity Read ↗

A retrospective analysis of amniocenteses performed for advanced maternal age and various other indications in Turkish womenSemantic proximity Read ↗

A multicenter study of fetal chromosomal abnormalities in Chinese women of advanced maternal ageSemantic proximity Read ↗

An overview of a 30-year experience with amniocentesis in a single tertiary medical center in TaiwanSemantic proximity Read ↗

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