Traduction de «Identify genetic disorders » (Anglais → Français) :

TERMINOLOGIE
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diagnose a genetic disease | identify genetic disorders | diagnose genetic diseases | diagnose genetic disorders

https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]

diagnostiquer des maladies génétiques

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

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déceler des troubles de l'apprentissage

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https://ec.europa.eu/esco/port (...) [HTML] [2017-12-31]

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

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traiter les troubles endocriniens

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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.

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syndrome lymphoprolifératif auto-immun avec infections virales récurrentes

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https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

genetic disease | genetic disorder

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

maladie génétique

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

diagnostic préimplantatoire | DPI

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

genetic disorder with high prevalence

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trouble génétique à forte prévalence

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http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

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

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déficit maternel en riboflavine

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https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

genetic disorder

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

trouble génétique

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

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

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syndrome de Warburg-Thomsen

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TRADUCTIONS EN CONTEXTE

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.

http://www.parl.gc.ca/HousePub (...) (...) [HTML] [2013-05-06]

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.

http://www.parl.gc.ca/HousePub (...) (...) [HTML] [2013-05-06]

http://www.parl.gc.ca/HousePub (...) [HTML] [2013-05-06]

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.

http://www.parl.gc.ca/HousePub (...) (...) [HTML] [2010-06-02]

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.

http://www.parl.gc.ca/HousePub (...) (...) [HTML] [2010-06-02]

http://www.parl.gc.ca/HousePub (...) [HTML] [2010-06-02]

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.

http://www.parl.gc.ca/HousePub (...) (...) [HTML] [2011-03-01]

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.

http://www.parl.gc.ca/HousePub (...) (...) [HTML] [2011-03-01]

http://www.parl.gc.ca/HousePub (...) [HTML] [2011-03-01]

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.

http://www.parl.gc.ca/Content/ (...) (...) [HTML] [1998-05-11]

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.

http://www.parl.gc.ca/Content/ (...) (...) [HTML] [1998-05-11]

http://www.parl.gc.ca/Content/ (...) [HTML] [1998-05-11]

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Date index: 2023-09-23