A subgroup of therapy-related myeloid neoplasms (t-MN), associated with treatment of an unrelated neoplastic disease with cytotoxic agents, like etoposide, doxorubicin, daunorubicin and others. The neoplastic cells often show rearrangements involving

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

leucémie aigüe myéloïde et syndromes myélodysplasiques liés aux inhibiteurs de la topoisomérase II

SNOMEDCT-BE (t-MN), associated with treatment of an unrelated neoplastic disease with cytotoxic agents, like etoposide, doxorubicin, daunorubicin and others. The neoplastic cells often show rearrangements involving / 766046007

SNOMEDCT-BE (disorder) / 766046007

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

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

rearrangement of staff [ staff rearrangement ]

http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]

remaniement de personnel

Transfer of Personnel

Mobilité du personnel

http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]

http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]

A very rare chromosomal anomaly in which both copies of chromosome 20 are inherited from the mother. The main feature described is prenatal and postnatal growth retardation. Microcephaly, minor dysmorphic features and psychomotor developmental delay

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

disomie uniparentale maternelle du chromosome 20

SNOMEDCT-BE (disorder) / 715735007

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

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

A rare chromosomal anomaly syndrome resulting from partial trisomy of the long arm of chromosome 20 with high phenotypic variability. The disease has characteristics of neurodevelopmental delay, cardiac malformations (ventricular septal defect, coarc

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

trisomie distale 20q

SNOMEDCT-BE (ventricular septal defect, coarc / 764500002

SNOMEDCT-BE (disorder) / 764500002

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

IN-CONTEXT TRANSLATIONS

The exact causes of the chromosomal rearrangement and primary prevention of Down's syndrome are still unknown.

http://www.parl.gc.ca/HousePub (...) (...) [HTML] [2014-09-10]

On ne connaît toujours pas les causes exactes de cette modification chromosomique et aucun moyen de prévention primaire n'est disponible pour l'instant.

http://www.parl.gc.ca/HousePub (...) (...) [HTML] [2014-09-10]

http://www.parl.gc.ca/HousePub (...) [HTML] [2014-09-10]

Chromosomal mutations generally involve parts of chromosomes which have been rearranged within the same chromosome or become attached to another chromosome or abnormal numbers of individual chromosomes or sets thereof.

http://www.europarl.europa.eu/ (...) (...) [HTML] [2001-11-07]

Généralement, les mutations chromosomiques sont constituées de parties chromosomiques redisposées, de quantités anormales de chromosomes individuels ou de quantités anormales de bagage génétique.

http://www.europarl.europa.eu/ (...) (...) [HTML] [2001-11-07]

http://www.europarl.europa.eu/ (...) [HTML] [2001-11-07]

www.wordscope.com (v4.0.br.77)

'chromosome rearrangement'

Date index:2021-03-24 -

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Translation of "chromosome rearrangement " (English → French) :

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