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Cooley's anemia
Cut filament
Cutting filament
Filament cutting
Hemoglobin S-thalassemia
Manage projects
Manage several projects
Managing several projects
Microdrepanocytic disease
Microdrepanocytosis
Oversee several projects
Sever filament
Severe ß thalassemia
Sickle cell-thalassemia
Sickle cell-thalassemia disease
Thalassemia-sickle cell disease
ß thalassanemia
ß thalassemia
ß-thalassemia
ßt
ß°-thalassemia

Translation of "severe ß thalassemia " (English → French) :

severe ß thalassemia [ Cooley's anemia ]

ß-thalassémie majeure [ anémie de Cooley ]
Blood
Sang


sickle cell-thalassemia disease | microdrepanocytosis | microdrepanocytic disease | hemoglobin S-thalassemia | sickle cell-thalassemia | thalassemia-sickle cell disease

maladie microdrépanocytaire
médecine
médecine


ß-thalassemia | ßt | ß thalassemia | ß thalassanemia

thalassémie ß | ß thalassémie | ß-thalassémie
médecine > sémiologie et pathologie
médecine > sémiologie et pathologie


ß°-thalassemia

thalassémie ß° | thalassémie Ferrare
médecine > sémiologie et pathologie
médecine > sémiologie et pathologie


manage projects | oversee several projects | manage several projects | managing several projects

gérer plusieurs projets à la fois
skill
Aptitude


Syndrome that is characterized by the association of multiple sclerosis with lamellar ichthyosis and hematological anomalies (beta thalassemia minor and a quantitative deficit of factor VIII-von Willebrand complex). Other clinical manifestations may

syndrome de sclérose en plaques-ichtyose-déficit en facteur VIII
SNOMEDCT-BE (beta thalassemia minor and a quantitative deficit of factor VIII-von Willebrand complex). Other clinical manifestations may / 733028000
SNOMEDCT-BE (disorder) / 733028000


A rare multiple malformation syndrome with characteristics of severe intrauterine growth retardation, severe microcephaly with a sloping forehead, severe ichthyosis (collodion baby type), and facial dysmorphism. Severe central nervous system defects

syndrome de Neu-Laxova
SNOMEDCT-BE (collodion baby type), and facial dysmorphism. Severe central nervous system defects / 77817004
SNOMEDCT-BE (disorder) / 77817004


A unique form of congenital adrenal hyperplasia characterised by glucocorticoid deficiency, severe sexual ambiguity in both sexes and skeletal (especially craniofacial) malformations. Prenatal androgen excess is responsible for severe virilisation of

hyperplasie congénitale des surrénales par déficit en cytochrome P450 oxydoréductase
SNOMEDCT-BE (especially craniofacial) malformations. Prenatal androgen excess is responsible for severe virilisation of / 715733000
SNOMEDCT-BE (disorder) / 715733000


filament cutting | sever filament | cut filament | cutting filament

couper des filaments
skill
Aptitude


A New Beginning - The Report of the Minister of Finance's Expert Panel on Financial Security for Children with Severe Disabilities

Un nouveau départ - Le rapport du Groupe d'experts du ministre des Finances au sujet de la sécurité financière des enfants gravement handicapés
Titles of Reports | Finance | Sociology of persons with a disability
Titres de rapports | Finances | Sociologie des personnes handicapées




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'severe ß thalassemia'

Date index:2023-11-18 -

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