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Antenatal screening for chromosomal anomalies
Chromosomal anomaly
Chromosomal replication
Chromosome anomaly
Chromosome duplication
Chromosome replication

Vertaling van "Chromosome anomaly " (Engels → Frans) :

TERMINOLOGIE


A rare chromosomal anomaly syndrome resulting from a partial interstitial deletion of the short arm of chromosome 9. The disease has characteristics of mild to moderate developmental delay, hand tremors, myoclonic jerks, attention deficit-hyperactivi

syndrome de microdélétion 9p13


A very rare chromosomal anomaly in which both copies of chromosome 20 are inherited from the mother. The main feature described is prenatal and postnatal growth retardation. Microcephaly, minor dysmorphic features and psychomotor developmental delay

disomie uniparentale maternelle du chromosome 20


A rare chromosomal anomaly syndrome resulting from partial trisomy of the long arm of chromosome 20 with high phenotypic variability. The disease has characteristics of neurodevelopmental delay, cardiac malformations (ventricular septal defect, coarc

trisomie distale 20q




Antenatal screening for chromosomal anomalies

Dépistage prénatal d'anomalies chromosomiques


chromosomal replication | chromosome duplication | chromosome replication

duplication des chromosomes | réplication des chromosomes
IN-CONTEXT TRANSLATIONS
It is now known that many individuals with chromosomal anomalies fail to survive birth. In other words, many chromosomal mutations cause a pregnancy to end before it has reached its full term, and only a small number of embryos with anomalies manage to survive.

On sait aujourd'hui que beaucoup d'anomalies chromosomiques ne survivent pas à la naissance, c'est-à-dire que de nombreuses mutations chromosomiques mettent précocement un terme à la grossesse et que peu d'embryons présentant des anomalies réussissent à survivre.




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Date index: 2024-11-16
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