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Anhidrotic ectodermal dysplasia
Chondroectodermal dysplasia
Christ-Siemens syndrome
Christ-Siemens-Touraine syndrome
Congenital ectodermal dysplasia
Craniometaphyseal dysplasia
Dysplasia of hip
EVC
Ectodermal dysplasia
Ellis-van Creveld syndrome
Hereditary ectodermal dysplasia
Hip dysplasia
Mesoectodermal dysplasia
Metaphyseal dysplasia
Pulpal
Pulpal cornua
Pulpal dysplasia
Pulpal horn
Pyle's disease
Siemens'syndrome

Traduction de «pulpal dysplasia » (Anglais → Français) :





hip dysplasia | dysplasia of hip

dysplasie de la hanche


anhidrotic ectodermal dysplasia | Christ-Siemens syndrome | hereditary ectodermal dysplasia | Christ-Siemens-Touraine syndrome

dysplasie ectodermique anhidrotique | dysplasie ectodermique | syndrome de Christ-Siemens | syndrome de Christ-Siemens-Touraine


craniometaphyseal dysplasia | metaphyseal dysplasia | Pyle's disease

dysplasie crânio-métaphysaire familiale | dysplasie métaphysaire familiale | maladie de Pyle


congenital ectodermal dysplasia | ectodermal dysplasia | Siemens'syndrome

syndrome de Christ-Siemens


chondroectodermal dysplasia | Ellis-van Creveld syndrome | mesoectodermal dysplasia | EVC [Abbr.]

chondrodysplasie chondroectodermique | syndrome d'Ellis-van Creveld




A rare genetic immuno-osseous dysplasia disorder with characteristics of pre and post-natal growth retardation, hypotonia, borderline to moderate intellectual disability, retinal dystrophy, spondyloepiphyseal dysplasia (epiphyseal dysplasia, epiphyse

syndrome de Roifman


Omodysplasia is a rare skeletal dysplasia characterised by severe limb shortening and facial dysmorphism. Two types of omodysplasia have been described: an autosomal recessive or generalised form (also referred to as micromelic dysplasia with disloca

omodysplasie




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

'pulpal dysplasia' ->

Date index: 2022-01-23
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