Syndrome de Robinow et brachydactylie de type B : un même gène, ROR2, à l'origine des deux phénotypes
- Other title
- Brachydactyly type B and Robinow syndrome : mutations of a single gene associated with two distinct phenotypes (en)
- Author
- GILGENKRANTZ, Simone
- Source
MS. Médecine sciences. 2000, Vol 16, Num 12, pp 1460-1461 ; ref : 9 ref
- ISSN
- 0767-0974
- Scientific domain
- General medicine general surgery
- Publisher
- EDK, Paris
- Publication country
- France
- Document type
- Article
- Language
- French
- Keyword (fr)
- Brachydactylie Cartilage Génétique Homme Lignée cellulaire Maladie héréditaire Membre supérieur Mutation Phénotype Robinow syndrome Récepteur orphelin Main pathologie Malformation Ostéochondrodysplasie Système ostéoarticulaire pathologie
- Keyword (en)
- Brachydactyly Cartilage Genetics Human Cell line Genetic disease Upper limb Mutation Phenotype Robinow syndrome Orphan receptor Disease of the hand Malformation Osteochondrodysplasia Diseases of the osteoarticular system
- Keyword (es)
- Braquidactilia Cartílago Genética Hombre Línea celular Enfermedad hereditaria Miembro superior Mutación Fenotipo Robinow síndrome Receptor huérfano Mano patología Malformación Osteocondrodisplasia Sistema osteoarticular patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B15 Diseases of the osteoarticular system / 002B15H Malformations and congenital and or hereditary diseases involving bones. Joint deformations
- Discipline
- Osteoarticular pathology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 808690
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.4267/10608/1610 
https://dx.doi.org/10.4267/10608/1610
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