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Translation of "gene-linked severe " (English → French) :

TERMINOLOGY
see also In-Context Translations below

bubble boy disease | X gene-linked severe combined immunodeficiency | X-linked SCID | X-linked severe combined immunodeficiency | X-SCID [Abbr.]

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

déficit immunitaire combiné sévère lié à une anomalie génétique sur le chromosome X | DICS-X [Abbr.]

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

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

sex linked gene | X-linked genes

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

gène lié au sexe | gène lié à l'X | gène lié au chromosome sexuel

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

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

sex-linked gene | X-linked gene

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

gène lié au sexe

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

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

An X-linked disorder of purine metabolism comprised of two forms: an early-onset severe form with characteristics of gout, urolithiasis, and neurodevelopmental anomalies (severe PRPP synthetase superactivity) and a mild late-onset form with no neurol

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

hyperactivité de la phosphoribosylpyrophosphate synthétase

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

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

A rare X-linked inherited type of ocular albinism described in one African kindred (7 males over 3 generations) to date with characteristics of severe visual impairment, translucent pale-blue irides, a reduction in the retinal pigment and moderately

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

albinisme oculaire avec surdité sensorielle tardive

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

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

Nephrotic syndrome with often-early onset defined by severe proteinuria with low serum albumin and possible oedema. This disease is rare but severe as it usually progresses to end-stage renal failure. Mutations in the NPHS2 gene (chromosome 1q25-q31

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

syndrome néphrotique idiopathique familial cortico-résistant

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

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

sex-linked gene

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

gène lié au sexe

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

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

linked gene

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

gènes liés

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

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

linked gene

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

gène lié

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

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

IN-CONTEXT TRANSLATIONS

This is very interesting because also shows us that HLA genes are not linked exclusively to immunity but also to angiogenesis and to several other regulatory functions.

http://www.parl.gc.ca/content/ (...) (...) [HTML] [2014-09-03]

C'est très intéressant, car nous apprenons ainsi que les gènes du système HLA ne commandent pas exclusivement le système immunitaire, mais aussi l'angiogenèse et d'autres fonctions régulatrices.

http://www.parl.gc.ca/content/ (...) (...) [HTML] [2014-09-03]

http://www.parl.gc.ca/Content/ (...) [HTML] [2014-09-03]

Others have searched : x gene-linked severe combined immunodeficiency x-scid x-linked scid x-linked gene x-linked genes x-linked severe combined immunodeficiency bubble boy disease linked gene sex linked gene sex-linked gene gene-linked severe

datacenter (1): www.wordscope.ca (v4.0.br)

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Date index: 2024-01-15