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Artificial chromosome
CMRNG
Chromosomal aberration
Chromosomal abnormality
Chromosomally resistant N. gonorrhoeae
Chromosomally resistant Neisseria gonorrhoeae
Chromosome aberration
Chromosome abnormality
Chromosome anomaly
Homolog
Homologous chromosome
Homologue
Matching chromosome
Synthesized chromosome
Synthetic chromosome

Translation of "homologous chromosome " (English → French) :

TERMINOLOGY
see also In-Context Translations below
homologous chromosome | matching chromosome

chromosome homologue
IATE - Health | Natural and applied sciences
IATE - Health | Natural and applied sciences


homologous chromosome

chromosome homologue
IATE - Health
IATE - Health


homolog | homologous chromosome | homologue

chromosomes homologues
IATE - Natural and applied sciences
IATE - Natural and applied sciences


chromosomal aberration | chromosomal abnormality | chromosome aberration | chromosome abnormality | chromosome anomaly

aberration chromosomique | anomalie chromosomique | aberration des chromosomes | remaniement chromosomique
biologie > génie génétique
biologie > génie génétique


CLBP (ClpB homolog, mitochondrial AAA ATPase chaperonin) deficiency

acidurie 3-méthylglutaconique type 7
SNOMEDCT-BE (ClpB homolog, mitochondrial AAA ATPase chaperonin) deficiency / 764860006
SNOMEDCT-BE (disorder) / 764860006


artificial chromosome | synthetic chromosome | synthesized chromosome

chromosome artificiel | chromosome synthétique | chromosome de synthèse
biologie > génie génétique | biologie > cytogénétique
biologie > génie génétique | biologie > cytogénétique


chromosome aberration | chromosomal aberration | chromosomal abnormality

aberration chromosomique
biologie > cytogénétique
biologie > cytogénétique


chromosomally resistant N. gonorrhoeae [ CMRNG | chromosomally resistant Neisseria gonorrhoeae ]

N. gonorrhoeae présentant une résistance d'ordre chromosomique [ NGRC | Neisseria gonorrhoeae présentant une résistance d'ordre chromosomique ]
Epidemiology
Épidémiologie


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
SNOMEDCT-BE (disorder) / 715735007
SNOMEDCT-BE (disorder) / 715735007


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
SNOMEDCT-BE (ventricular septal defect, coarc / 764500002
SNOMEDCT-BE (disorder) / 764500002
IN-CONTEXT TRANSLATIONS
Every individual inherits two sets of chromosomes and hence two sets of homologous genes.

Chaque individu hérite de deux séries de chromosomes et donc de deux ensembles de gènes homologues.




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'homologous chromosome'

Date index:2022-01-13 -

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