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Congenital absence of vertebra
Fusion of spine
Hemivertebra
Joint Indian Association Committee of Chiefs of Ontario
Joint Indian Association Committee of Ontario
Joint associates
Joint stock association
Joint stock company
Joint-stock association
Kyphosis
Lordosis
Malformation of lumbosacral
Malformation of spine
Platyspondylisis
Stock association
Supernumerary vertebra
Unspecified or not associated with scoliosis

Vertaling van "nd joint association " (Engels → Frans) :



joint stock association | joint-stock association

association de capitaux


Joint Committee EEC-European Free Trade Association - Joint Transit

Commission mixte CEE-Association européenne de libre-échange - transit commun


joint stock association [ joint-stock association ]

association de capitaux


Joint Indian Association Committee of Chiefs of Ontario [ Joint Indian Association Committee of Ontario ]

Comité conjoint de l'association des chefs de l'Ontario


joint stock company | joint-stock association | stock association

société par actions à responsabilité illimitée


Joint Committee EEC-European Free Trade Association - Single Document

Commission mixte CEE-Association européenne de libre-échange - document unique


Congenital:absence of vertebra | fusion of spine | kyphosis | lordosis | malformation of lumbosacral (joint) (region) | Hemivertebra | Malformation of spine | Platyspondylisis | Supernumerary vertebra | unspecified or not associated with scoliosis

Absence congénitale de vertèbres | Cyphose congénitale | Hémivertèbre [hémispondylie] | Lordose congénitale | Malformation congénitale (charnière) de la région lombo-sacrée | Malformation du rachis | Platyspondylie | Synostose vertébrale congénitale | Vertèbre surnuméraire | sans précision ou non associée à une scoliose


A very rare multiple congenital anomalies syndrome described in three brothers of one South-African family, and with features of hypospadias and intellectual deficit, in association with microcephaly, craniofacial dysmorphism, joint laxity and beaked

syndrome d'hypospadias-déficience intellectuelle type Goldblatt


A rare genetic motor neuron disease with characteristics of progressive early respiratory failure associated with diaphragm paralysis, distal muscular weakness, joint contractures, and axial hypotonia with preserved antigravity limb movements. The ph

amyotrophie spinale diaphragmatique type 2




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Date index: 2021-10-01
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