Boost Your Productivity!Translate documents (Ms-Word, Ms-Excel, ...) faster and better thanks to artificial intelligence!
https://pro.wordscope.com
https://blog. wordscope .com
Anhidrotic ectodermal dysplasia
Canadian Society for Ectodermal Dysplasias
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
M.E.D.
MED
Mesoectodermal dysplasia
Metaphyseal dysplasia
Multiple Epiphyseal Dysplasia
Multiple epiphyseal dysplasia
Pyle's disease
Siemens'syndrome

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

craniometaphyseal dysplasia | metaphyseal dysplasia | Pyle's disease

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


Craniometaphyseal dysplasia

dysplasie cranio-métaphysaire


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


hip dysplasia | dysplasia of hip

dysplasie de la hanche


multiple epiphyseal dysplasia | M.E.D. | MED | Multiple Epiphyseal Dysplasia

dysplasies épiphysaires multiples | dysplasies polyépiphysaires


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

chondrodysplasie chondroectodermique | syndrome d'Ellis-van Creveld


congenital ectodermal dysplasia | ectodermal dysplasia | Siemens'syndrome

syndrome de Christ-Siemens


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


Canadian Society for Ectodermal Dysplasias

Canadian Society for Ectodermal Dysplasias


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)

'craniometaphyseal dysplasia' ->

Date index: 2022-09-14
w