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ACC
Agenesis of the corpus callosum
Aicardi syndrome
Asplenia syndrome
Dysplasia renal facialis
Ivemark's syndrome
Polhemus-Schafer-Ivemark syndrome
Potter's syndrome
Renal agenesis syndrome
Renofacial syndrome
Splenic agenesis syndrome
Splenic deficiency syndrome
XY Gonadal agenesis syndrome

Traduction de «splenic agenesis syndrome » (Anglais → Français) :

Ivemark's syndrome | Polhemus-Schafer-Ivemark syndrome | asplenia syndrome | splenic agenesis syndrome

syndrome de Ivemark | asplénisme congénital


Potter's syndrome | renofacial syndrome | renal agenesis syndrome | dysplasia renal facialis

syndrome de Potter


splenic deficiency syndrome

syndrome de déficience splénique


splenic deficiency syndrome

syndrome de déficience splénique


XY Gonadal agenesis syndrome

anorchidie congénitale isolée


agenesis of the corpus callosum | Aicardi syndrome | ACC [Abbr.]

syndrome d'Aicardi


A rare developmental defect during embryogenesis syndrome, with characteristics of normal female karyotype, normal ovaries, male or ambiguous genitalia, urinary tract malformations (ranging from bilateral renal agenesis to mild unilateral hydronephro

syndrome d'anomalie du développement sexuel 46,XX-anomalies anorectales


Agenesis of nerve Displacement of brachial plexus Jaw-winking syndrome Marcus Gunn's syndrome

Agénésie d'un nerf Anomalie d'un plexus nerveux Mâchoire à clignement Phénomène de Marcus Gunn


Disease with characteristics of progressive ataxia beginning during infancy, a pyramidal syndrome and dental agenesis. The syndrome has been described in four children born to consanguineous parents. The mode of transmission is autosomal recessive.

odontoleucodystrophie




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Date index: 2021-08-25
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