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Autosomaal recessieve aplasia cutis
Autosomaal recessieve cutis laxa type 2B
Chalastoderma
Chalastodermia
Chalazoderma
Chalazodermia
Chaloderma
Chalodermie
Cutis laxa
Cutis laxa senilis
Cutis pendula
Cutis rhomboidalis nuchae
Dermatolyse
Dermatolysis
Pachydermatocele
Pachydermatokèle
Pollenallergeen van Betula pendula
Xerosis cutis

Traduction de «cutis pendula » (Néerlandais → Anglais) :



chalastoderma | chalastodermia | chalazodermia | cutis laxa | cutis pendula | dermatolyse | dermatolysis | pachydermatocele

dermatolysis


chalastodermia | chalazoderma | chalazodermia | chaloderma | chalodermie | cutis laxa | cutis pendula | dermatolyse | dermatolysis | pachydermatokèle

chalazodermia | cutis laxa | dermatolysis | loose skin | pachydermatocele


pollenallergeen van Betula pendula

Silver birch pollen allergen


autosomaal recessieve aplasia cutis

An extremely rare association syndrome, described in only two brothers to date (one of which died at 2 months of age), characterised by aplasia cutis congenita of the vertex and generalised oedema (as well as hypoproteinaemia and lymphopenia) due to


autosomaal recessieve cutis laxa type 2B

Autosomal recessive cutis laxa type 2B










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Date index: 2024-04-01
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