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DNA library
Dementia in Huntington's chorea
Gene
Gene bank
Gene banks
Gene library
Gene pool
Genetic catalogue
Genetic data bank
Genetic data base
Genetic databank
Genetic database
Genetic information database
Genetic resource
Genetic stock
Genetics
Genomic library
Genotype
Heredity
NF-1 gene
NF-2 gene
Neurofibroma
Neurofibroma-1 gene
Neurofibroma-2 gene
Nuclear gene
T

Translation of "neurofibroma-2 gene " (English → French) :

neurofibroma-2 gene | NF-2 gene

gène NF-2
IATE - Health
IATE - Health


neurofibroma-1 gene | NF-1 gene

gène NF-1
IATE - Health
IATE - Health


Ovarian cancer caused by germline mutations in various genes, usually associated with additional cancer risks. The most common are breast and ovarian cancer syndrome (HBOC) due to mutations in BRCA1 and BRCA2 genes and hereditary nonpolyposis colorec

syndrome héditaire de prédisposition au cancer de l'ovaire
SNOMEDCT-BE (HBOC) due to mutations in BRCA1 and BRCA2 genes and hereditary nonpolyposis colorec / 771080008
SNOMEDCT-BE (disorder) / 771080008


Describes a rare group of immunodeficiencies due to specific mutations in the inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma (IKBKG) or the cytochrome b-245, beta polypeptide (CYBB) genes. The clinical manifestation is my

prédisposition mendélienne liée à l'X aux infections mycobactériennes
SNOMEDCT-BE (IKBKG) or the cytochrome b-245, beta polypeptide (CYBB) genes. The clinical manifestation is my / 719814009
SNOMEDCT-BE (disorder) / 719814009


genetic database [ DNA library | gene bank | gene library | genetic catalogue | genetic databank | genetic data bank | genetic data base | genetic information database | genomic library | [http ...]

base de données génétiques [ banque de données génétiques | banque de gènes | banque de génomes | banque d’ADN | base de données et d'informations sur les gènes | bibliothèque de gènes | catalogue des gènes | génothèque ]
36 SCIENCE | MT 3606 natural and applied sciences | BT1 genetics | BT2 biology | BT3 life sciences | RT database [3236]
36 SCIENCES | MT 3606 sciences naturelles et appliquées | BT1 génétique | BT2 biologie | BT3 sciences de la vie | RT base de données [3236]




A rare subtype of renal cell carcinoma with recurrent genetic abnormalities, harboring rearrangements of the TFE3 (Xp11 t-RCC) or TFEB [t(6; 11) t-RCC] genes. The t(6; 11) t-RCC has distinctive histologic features of biphasic appearance with larger epi

carcinome rénal associé à une translocation de la famille MiT
SNOMEDCT-BE (Xp11 t-RCC) or TFEB [t(6;11) t-RCC] genes. The t(6;11) t-RCC has distinctive histologic features of biphasic appearance with larger epi / 764694005
SNOMEDCT-BE (disorder) / 764694005


nuclear gene (1) | gene (2)

gène nucléaire
Medicine & biology
Physiologie (Sciences médicales et biologiques) | Biologie (Sciences médicales et biologiques)


Definition: A dementia occurring as part of a widespread degeneration of the brain. The disorder is transmitted by a single autosomal dominant gene. Symptoms typically emerge in the third and fourth decade. Progression is slow, leading to death usually within 10 to 15 years. | Dementia in Huntington's chorea

Définition: Démence survenant dans le contexte d'une dégénérescence cérébrale étendue. La maladie est transmise par un gène autosomique dominant unique. Les symptômes apparaissent typiquement dans la troisième et la quatrième décennies. L'évolution est lentement progressive, aboutissant habituellement à la mort en 10 à 15 années. | Démence de la chorée de Huntington
WORLD HEALTH ORGANIZATION ICD-10: F02.2*
WORLD HEALTH ORGANIZATION ICD-10: F02.2*


genetics [ gene pool | genetic resource | genetic stock | genotype | heredity | heredity(UNBIS) ]

génétique [ hérédité | patrimoine génétique | ressource génétique ]
36 SCIENCE | MT 3606 natural and applied sciences | BT1 biology | BT2 life sciences | NT1 DNA | NT1 eugenics | NT1 genetic database | RT genetic engineering [6411]
36 SCIENCES | MT 3606 sciences naturelles et appliquées | BT1 biologie | BT2 sciences de la vie | NT1 ADN | NT1 base de données génétiques | NT1 eugénique | RT génie génétique [6411]




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'neurofibroma-2 gene'

Date index:2023-08-18 -

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