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Ascertain learning disorders
BABI
Blastomer analysis before implantation
Diagnose a genetic disease
Diagnose genetic diseases
Diagnose genetic disorders
Embryo genetic disorder analysis
Genetic disease
Genetic disorder
Genetic disorder with high prevalence
Identify endocrine disorders
Identify genetic disorders
Identify learning disorder
Identify learning disorders
Identifying learning disorders
PGD
PIGD
Pre-implantation genetic diagnosis
Preimplantation genetic diagnosis
Treat endocrine disorders
Treat glucose homeostasis disorders
Treat menstrual disorders

Translation of "identify genetic disorders " (English → French) :

TERMINOLOGY
see also In-Context Translations below
diagnose a genetic disease | identify genetic disorders | diagnose genetic diseases | diagnose genetic disorders

diagnostiquer des maladies génétiques
skill
Aptitude


identify learning disorder | identifying learning disorders | ascertain learning disorders | identify learning disorders

déceler des troubles de l'apprentissage
skill
Aptitude


treat glucose homeostasis disorders | treat menstrual disorders | identify endocrine disorders | treat endocrine disorders

traiter les troubles endocriniens
skill
Aptitude


A rare genetic disorder with characteristics of lymphadenopathy and/or splenomegaly and recurrent infections due to herpes viruses. Prevalence of this disorder is not known. It is extremely rare with four individuals in one family identified to date.

syndrome lymphoprolifératif auto-immun avec infections virales récurrentes
SNOMEDCT-BE (disorder) / 722290008
SNOMEDCT-BE (disorder) / 722290008


genetic disease | genetic disorder

maladie génétique
IATE - Health
IATE - Health


preimplantation genetic diagnosis | PGD | pre-implantation genetic diagnosis | PIGD | embryo genetic disorder analysis | blastomer analysis before implantation | BABI

diagnostic préimplantatoire | DPI
biologie > génétique | médecine > gynécologie et obstétrique
biologie > génétique | médecine > gynécologie et obstétrique


genetic disorder with high prevalence

trouble génétique à forte prévalence
IATE - Health
IATE - Health


A rare genetic disorder of metabolite absorption or transport with characteristics of persistently decreased riboflavin serum levels due to a primary genetic defect in the mother and which leads to clinical and biochemical findings consistent with a

déficit maternel en riboflavine
SNOMEDCT-BE (disorder) / 773549000
SNOMEDCT-BE (disorder) / 773549000


genetic disorder

trouble génétique
sociologie > gérontologie
sociologie > gérontologie


An exceedingly rare genetic disorder with characteristics of cutaneous pigmentation anomalies, ocular disorders and hearing loss. The syndrome was described in 1990 in two patients from the same Yemenite family. A brother and sister were described as

syndrome de Warburg-Thomsen
SNOMEDCT-BE (disorder) / 721084001
SNOMEDCT-BE (disorder) / 721084001
IN-CONTEXT TRANSLATIONS
Through remarkable collaboration of all genetic centres in Canada, this group was able to identify over 180 rare pediatric genetic disorders affecting hundreds of children in Canada and internationally.

Grâce à la collaboration remarquable de tous les centres de génétique du Canada, ce groupe a réussi à identifier plus de 180 troubles génétiques rares qui touchaient des centaines d'enfants canadiens et étrangers.


Internationally, newborn screening is becoming one of the most important ways of identifying genetic disorders, many of which, in fact, if they were caught at birth, could be treated from birth without the devastating effects.

À l'échelle internationale, le dépistage néonatal est en voie de devenir l'une des méthodes les plus importantes de dépistage des troubles génétiques, dont beaucoup en fait peuvent être traités immédiatement et sans effet dévastateur s'ils sont décelés à la naissance.


My own belief, and it's really my own belief again, I am not an expert on this topic is that epigenetics and genetics studies will help us screen and identify the individuals who have an increased susceptibility to developing this type of disorder.

Personnellement, je suis d'avis — et je le répète, je ne suis pas expert en la matière — que les études en épigénétique et en génétique nous aideront à dépister ce type de trouble et à identifier les personnes portées à le développer.


Murray Barr identified a sex chromatin body, the Barr body, and launched a new era of research and diagnosis of genetic disorders, especially those associated with mental retardation.

Murray Barr a identifié une chromatine sexuelle, le corps de Barr. Il a lancé une nouvelle ère de recherche et de diagnostic des troubles génétiques, surtout ceux associés à l'arriération mentale.




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'identify genetic disorders'

Date index:2024-04-27 -

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