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

Cytogenetic diagnosis of “normal 46,XX” karyotypes in spontaneous abortions frequently may be misleading

1 Feb 1999

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 Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Share to Gynecological conditions and treatments
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 9988408
DOI: 10.1016/s0015-0282(98)00445-2

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

Cytogenetic diagnosis of “normal 46,XX” karyotypes in spontaneous abortions frequently may be misleadingPMID 9988408Read ↗

Incidence and spectrum of chromosome abnormalities in spontaneous abortions: New insights from a 12-year studySemantic proximity Read ↗

Turner syndrome phenotype with 47,XXX karyotype: further investigation warranted?Semantic proximity Read ↗

Characteristics of chromosomal abnormalities diagnosed after spontaneous abortions in an infertile populationSemantic proximity Read ↗

Karyotype evaluation of repeated abortions in primary and secondary recurrent pregnancy lossSemantic proximity Read ↗

Chromosomal abnormalities of 19,000 couples with recurrent spontaneous abortions: a multicenter studySemantic proximity Read ↗

Complete gonadal dysgenesis in clinical practice: the 46,XY karyotype accounts for more than one third of casesSemantic proximity Read ↗

Mosaic 46,XX,der(9)t(9;13)(p24;q12)/46,XX at amniocentesis can be a culture artefact and associated with a favorable fetal outcomeSemantic proximity Read ↗

The smaller than expected first-trimester fetus is at increased risk for chromosome anomaliesSemantic proximity Read ↗

Chromosome abnormalities identified in 457 spontaneous abortions and their histopathological findings.Semantic proximity Read ↗

Reliability of 46,XX results on miscarriage specimens: a review of 1,222 first-trimester miscarriage specimensSemantic proximity Read ↗

Tissue Sampling Technique Affects Accuracy of Karyotype from Missed AbortionsSemantic proximity Read ↗

Cytogenetic analysis of 1508 spontaneous abortions originating from south SlovakiaSemantic proximity Read ↗

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