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BABI
Blastomer analysis before implantation
Determine mental disorders
Diagnose a genetic disease
Diagnose communication disorders
Diagnose genetic diseases
Diagnose genetic disorders
Diagnose mental disorders
Diagnose patients with emotional disorders
Diagnose patients with mental health disorders
Diagnose speech and communication disorders
Diagnose speech disorders
Embryo genetic disorder analysis
Genetic disease
Genetic disorder
Genetic disorder with high prevalence
Identify genetic disorders
Identify speech disorders
PGD
PIGD
Pre-implantation genetic diagnosis
Preimplantation genetic diagnosis
Sex-linked genetic disorder

Übersetzung für "Diagnose genetic disorders " (Englisch → Französisch) :

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

diagnostiquer des maladies génétiques


diagnose communication disorders | diagnose speech and communication disorders | diagnose speech disorders | identify speech disorders

diagnostiquer des troubles du langage


determine mental disorders | diagnose patients with mental health disorders | diagnose mental disorders | diagnose patients with emotional disorders

diagnostiquer des troubles mentaux




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

diagnostic préimplantatoire | DPI


genetic disorder with high prevalence

trouble génétique à forte prévalence


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


sex-linked genetic disorder

maladie héréditaire liée au sexe | maladie dont la transmission est liée au sexe




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
IN-CONTEXT TRANSLATIONS
Nicholas and Jonathan are 10-year-olds living in Ontario and diagnosed with Prader-Willi Syndrome, a rare genetic disorder resulting in multiple symptoms but most frequently includes morbid obesity because of insatiable appetite, intellectual disability and short stature due to low levels of growth hormone.

Nicholas et Jonathan sont des enfants de 10 ans qui vivent en Ontario et qui sont atteints du syndrome de Prader- Willi, une maladie génétique rare à multiples symptômes, qui comprend fréquemment l'obésité morbide à cause d'un appétit insatiable, une déficience intellectuelle et une petite taille à cause de faibles niveaux d'hormones de croissance.


– postnatal diagnostics is used to diagnose a disease, determine the probability that an infant will develop a given disease, the onset of which does not occur until later in life, and detect genetic alterations that increase the predisposition to some illnesses such as certain tumours and cardiovascular disorders;

- le diagnostic postnatal est utilisé pour diagnostiquer une pathologie, la probabilité d'apparition tardive d'une pathologie déterminée et la présence d'altérations génétiques qui augmentent la prédisposition à certaines maladies, comme certaines néoplasies et pathologies cardiovasculaires;


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