Pascal and Francis Bibliographic Databases

Help

Export

Selection :

Permanent link
http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3218562

Positional cloning of a gene involved in hereditary multiple exostoses

Author
WUYTS, W1 ; VAN HUL, M1 ; BOSSUYT, P2 ; BALEMANS, W2 ; FRANSEN, E2 ; VITS, L2 ; COUCKE, P2 ; NOWAK, N. J; SHOWS, T. B; MALLET, L5 ; VAN DEN OUWELAND, A. M. W4 ; MCGAUGHRAN, J6 ; WAUTERS, J1 ; HALLEY, D. J. J4 ; WILLEMS, P. J2 ; NEMTSOVA, M3 ; REYNIERS, E1 ; VAN HUL, E1 ; DE BOULLE, K1 ; DE VRIES, B. B. A4 ; HENDRICKX, J1 ; HERRYGERS, I1
[1] Department of Medical Genetics, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium
[2] Department of Medical Genetics, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium
[3] Research Center for Medical Genetics, Russian Academy of Medical Sciences, Moscow, Russian Federation
[4] Department of Clinical Genetics, Erasmus University, Rotterdam, Netherlands
[5] Department of Human Genetics, Roswell Park Cancer Institute, Buffalo, NY, United States
[6] Unité de Recherches sur les Handicaps Génétiques de l'Enfant, Inserm U393, Hôpital des Enfants-Malades, Paris, France
Source

Human molecular genetics (Print). 1996, Vol 5, Num 10, pp 1547-1557 ; ref : 48 ref

ISSN
0964-6906
Scientific domain
Genetics
Publisher
Oxford University Press, Oxford
Publication country
United Kingdom
Document type
Article
Language
Russian
Keyword (fr)
Carte génétique Carte physique Chromosome C11 Contig DNA complémentaire Délétion Exostose maladie Expression génique Gène Génétique Homme Homologie Mutation Séquence nucléotide Maladie héréditaire Ostéochondrodysplasie Système ostéoarticulaire pathologie
Keyword (en)
Genetic mapping Physical map Chromosome C11 Contig Complementary DNA Deletion Multiple cartilaginous exostosis Gene expression Gene Genetics Human Homology Mutation Nucleotide sequence Genetic disease Osteochondrodysplasia Diseases of the osteoarticular system
Keyword (es)
Mapa genético Mapa físico Cromosoma C11 Contig DNA complementario Deleción Exóstosis múltiple cartilaginosa Expresión genética Gen Genética Hombre Homología Mutación Secuencia nucleótido Enfermedad hereditaria 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
3218562

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

Access to the document

Searching the Web