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

Clinical relevance of diagnosing structural chromosome abnormalities in couples with repeated miscarriage.

Human reproduction (Oxford, England) - 1 Apr 2004

Goddijn M, Joosten J H K, Knegt A C, van derVeen F, Franssen M T M, Bonsel G J, Leschot N J

Abstract excerpt

BACKGROUND: The annual number of parental karyotypes in cases of repeated miscarriage is increasing gradually in The Netherlands. The efficiency of offering parental karyotyping in couples with repeated miscarriage has not been evaluated before, especially not for the group with miscarriages at advanced maternal age. METHODS: A historical cohort study and nested case-control study were conducted, including...

Read the complete abstract on PubMed

Topics

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

Share to Abortion, Habitual
Share to Chromosome Aberrations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cohort Studies

Share to Genetic Testing

Share to Karyotyping

Share to Maternal Age

Share to Pregnancy

Share to Risk Assessment

Source

Identifiers

PMID: 14990541
DOI: 10.1093/humrep/deh172

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical relevance of diagnosing structural chromosome abnormalities in couples with repeated miscarriage.PMID 14990541Read ↗

Consecutive or non-consecutive recurrent miscarriage: is there any difference in carrier status?Semantic proximity Read ↗

[Risk factors for structural chromosomal abnormality in > or = 2 miscarriages, as an instrument for selective karyotyping].Semantic proximity Read ↗

Reproductive outcome after chromosome analysis in couples with two or more miscarriages: case-control studySemantic proximity Read ↗

Selective chromosome analysis in couples with two or more miscarriages: case-control studySemantic proximity Read ↗

The effect of maternal age on chromosomal anomaly rate and spectrum in recurrent miscarriageSemantic proximity Read ↗

Genetic causes of recurrent miscarriages.Semantic proximity Read ↗

Reproductive outcome and fetal karyotype of couples with recurrent miscarriages.Semantic proximity Read ↗

Cytogenetic analysis of miscarriages from couples with recurrent miscarriage: a case-control studySemantic proximity Read ↗

Chromosomal abnormalities in couples with repeated fetal loss: An Indian retrospective studySemantic proximity Read ↗

Analysis of Parental Abnormal Chromosomal Karyotype and Subsequent Live Births in Chinese Couples with Recurrent MiscarriageSemantic proximity Read ↗

Subsequent pregnancy outcomes in recurrent miscarriage patients with a paternal or maternal carrier of a structural chromosome rearrangementSemantic proximity Read ↗

Analysis of Parental Abnormal Chromosomal Karyotype and Subsequent Live Births in Chinese Couples With Recurrent MiscarriageSemantic proximity Read ↗

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