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Adenomatous polyposis coli
Apartment block
Apartment building
Apartment dwelling
Apartment house
Block of flats
FAP
Familial adenomatous polyposis
Familial intestinal polyposis
Familial polyposis
Familial polyposis coli
Flat house
Gene family
Multi-family dwelling
Multi-occupancy block
Multifamily dwelling
Multiple dwelling
Multiple dwelling structure
Multiple familial polyposis
Multiple family dwelling
Multiple genes
Multiple-family dwelling
Polyposis coli
Residential build

Traduction de «multiple familial polyposis » (Anglais → Français) :

familial polyposis [ polyposis coli | familial intestinal polyposis | multiple familial polyposis ]

polypose colique familiale [ adénomatose du gros intestin ]


familial adenomatous polyposis | FAP | familial polyposis coli | familial intestinal polyposis | adenomatous polyposis coli

polypose adénomateuse familiale | PAF | polypose adénomateuse colique familiale | polypose colique familiale | polypose rectocolique familiale


familial adenomatous polyposis | familial polyposis | FAP [Abbr.]

polypose recto-colique


apartment building [ apartment dwelling | apartment house | flat house | apartment block | block of flats | multiple dwelling | multifamily dwelling | multi-family dwelling | multiple-family dwelling | multiple family dwelling | multiple dwelling structure | multi-occupancy block | residential build ]

immeuble d'habitation [ immeuble résidentiel | immeuble à usage d'habitation | immeuble collectif | habitation collective | habitation multifamiliale | bâtiment résidentiel | immeuble d'appartements | maison d'appartements | maison à appartements | maison à logements | immeuble domiciliaire | bloc à ]




Cap polyposis (CP) is characterised by multiple inflammatory polyps that predominantly affect the rectosigmoid area and manifest primarily as rectal bleeding with abnormal transit, constipation or diarrhoea. To date, around 67 cases have been describ

cap polypose


A rare familial skeletal dysplasia with characteristics of multiple epiphyseal dysplasia with extremely retarded ossification. It has been described in 6 members of a unique consanguineous family. A mutation in PTHR1 gene is responsible for this synd

syndrome d'Eiken


gene family | multiple genes

famille de gènes | famille multigénique


gene family | multiple genes

famille de gènes | famille multigénique


gene family | multiple genes

famille de gènes | famille multigénique




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Date index: 2023-12-25
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