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

Nederlands tijdschrift voor geneeskunde - 14 Apr 2007

Franssen M T M, Korevaar J C, Leschot N J, Bossuyt P M M, Knegt A C, Gerssen-Schoorl K B J, Wouters C H, Hansson K B M, Hochstenbach P F R, Madan K, van der Veen F, Goddijn M

Abstract excerpt

OBJECTIVE: To identify additional risk factors and the corresponding probability of carrying a chromosome abnormality in couples with two or more miscarriages. DESIGN: Nested case-control study. METHOD: In 6 centres for clinical genetics in the Netherlands, data were collected from couples referred for karyotyping after 2 2 miscarriages from 1992-2000. Factors influencing the probability of carrier status were...

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PMID: 17472118

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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.

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