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Hemoglobin S-thalassemia
Heterozygous
Heterozygous species
Heterozygous thalassemia
Mediterranean Committee for Thalassemia
Microdrepanocytic disease
Microdrepanocytosis
Sickle cell-thalassemia
Sickle cell-thalassemia disease
Thalassemia Foundation of Canada
Thalassemia-sickle cell disease
ß thalassanemia
ß thalassemia
ß-thalassemia
ßt
α+-thalassemia
α-thalassemia 2

Traduction de «Heterozygous thalassemia » (Anglais → Français) :



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

maladie microdrépanocytaire




ß-thalassemia | ßt | ß thalassemia | ß thalassanemia

thalassémie ß | ß thalassémie | ß-thalassémie




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




Thalassemia Foundation of Canada

Fondation canadienne de la thalassémie


Mediterranean Committee for Thalassemia

Mediterranean Committee for Thalassemia


A very rare form of multiple endocrine neoplasia, an inherited cancer syndrome, with parathyroid and anterior pituitary tumors, possibly associated with adrenal, renal, and reproductive organ tumors. Caused by heterozygous inactivating mutations in t

néoplasie endocrinienne multiple type 4




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

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Date index: 2024-03-09
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