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Bessel-Hagen disease
Chondrodysplasia
Chondrodysplasia punctata
Giant cell chondrodysplasia
Hereditary deforming chondrodysplasia
Hereditary multiple exostosis
Metaphyseal chondrodysplasia Kaitila type
Multiple cartilaginous exostoses
Multiple exostosis
Multiple osteochondromas

Traduction de «chondrodysplasia » (Anglais → Néerlandais) :





Bessel-Hagen disease | hereditary deforming chondrodysplasia | hereditary multiple exostosis | multiple cartilaginous exostoses | multiple exostosis | multiple osteochondromas

heriditaire multiple exostose | multiple erfelijk osteochondroom | HME [Abbr.]




An extremely rare disorder of sex development, reported in only two siblings to date. The syndrome has clinical features of 46,XY complete gonadal dysgenesis in association with severe dwarfism with generalised chondrodysplasia (bell-shaped thorax, m

syndroom van Nivelon-Nivelon-Mabille


Metaphyseal chondrodysplasia Kaitila type

metafysaire chondrodysplasie, Kaitila-type




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Date index: 2024-01-07
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