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Aarskog
Acrocefalopolysyndactylie
Acrocefalosyndactylie
Apert
Cockayne
Cryptoftalmiesyndroom
Cyclopie
De Lange
Dubowitz
Goldenhar
Holt-Oram
Klippel-Trenaunay-Weber
Möbius
Nagel-patella
Noonan
Oro-faciaal-digitaalsyndroom
Prader-Willi
Robin
Robin-syndroom
Robinow-Silverman-Smith
Rubinstein-Taybi
Russell-Silver
Seckel
Sirenomelie
Smith-Lemli-Opitz
Syndroom
Syndroom
Syndroom van
Syndroom van Abderhalden-Fanconi
Syndroom van Bernard
Syndroom van Debré-Fanconi
Syndroom van Debré-de Toni-Fanconi
Syndroom van Horner
Syndroom van Horner-Bernard
TAR-syndroom
Trombocytopenie met ontbreken van radius
VATER-syndroom
Whistling face
Ziektebeeld

Traduction de «Robin-syndroom » (Néerlandais → Anglais) :

Robin-syndroom

Pierre Robin syndrome | Robin anomalad | Robin's syndrome


acrocefalopolysyndactylie | acrocefalosyndactylie [Apert] | cryptoftalmiesyndroom | cyclopie | oro-faciaal-digitaalsyndroom | syndroom van | Goldenhar | syndroom van | Möbius | syndroom van | Robin | whistling face

Acrocephalopolysyndactyly Acrocephalosyndactyly [Apert] Cryptophthalmos syndrome Cyclopia Syndrome:Goldenhar | Moebius | oro-facial-digital | Robin | Whistling face


intellectuele achterstand, brachydactylie, syndroom van Pierre Robin

A rare developmental defect during embryogenesis with characteristics of mild to moderate intellectual disability and psychomotor delay, Robin sequence (including severe micrognathia and soft palate cleft) and distinct dysmorphic facial features (e.g


syndroom van ventriculaire extrasystolie met syncope, congenitale anomalie van digitus en sequentie van Robin

Stoll Kieny Dott syndrome


syndroom van kleine gestalte, Pierre Robin-sequentie, gespleten onderkaak, misvormingen van hand en klompvoet

Syndrome with characteristics of short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies (including hypoplastic thumbs) and clubfoot. It has been described in 14 Brazilian families and in one unrelated French patient. Prominent lo




syndroom van Abderhalden-Fanconi | syndroom van Debré-de Toni-Fanconi | syndroom van Debré-Fanconi

A.-F.syndrome | cystine storage disease


syndroom van Bernard | syndroom van Horner | syndroom van Horner-Bernard

Bernard-Horner syndrome


syndroom van | Aarskog | syndroom van | Cockayne | syndroom van | de Lange | syndroom van | Dubowitz | syndroom van | Noonan | syndroom van | Prader-Willi | syndroom van | Robinow-Silverman-Smith | syndroom van | Russell-Silver | syndroom van | Seckel | syndroom van | Smith-Lemli-Opitz

Syndrome:Aarskog | Cockayne | De Lange | Dubowitz | Noonan | Prader-Willi | Robinow-Silverman-Smith | Russell-Silver | Seckel | Smith-Lemli-Opitz


syndroom (van) | Holt-Oram | syndroom (van) | Klippel-Trenaunay-Weber | syndroom (van) | nagel-patella | syndroom (van) | Rubinstein-Taybi | syndroom (van) | sirenomelie | TAR-syndroom [trombocytopenie met ontbreken van radius] | VATER-syndroom

Syndrome:Holt-Oram | Klippel-Trénaunay-Weber | nail patella | Rubinstein-Taybi | sirenomelia | thrombocytopenia with absent radius [TAR] | VATER




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Date index: 2021-05-08
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