Recessive inheritance of von Willebrand's disease type I
- Author
- EIKENBOOM, J. C. J; REITSMA, P. H; PEERLINCK, K. M. J; BRIËT, E
Univ. hosp. Leiden, haemostasis thrombosis res. cent., dep. haematology, 2300 RC Leiden, Netherlands - Source
Lancet (British edition). 1993, Vol 341, Num 8851, pp 982-986 ; ref : 26 ref
- CODEN
- LANCAO
- ISSN
- 0140-6736
- Scientific domain
- General medicine general surgery
- Publisher
- Lancet, London
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Coagulopathie Cytogénétique Exploration Homme Maladie héréditaire Willebrand maladie Hémopathie
- Keyword (en)
- Coagulopathy Cytogenetics Exploration Human Genetic disease Willebrand disease Hemopathy
- Keyword (es)
- Coagulopatía Citogenética Exploración Hombre Enfermedad hereditaria Willebrand enfermedad Hemopatía
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B19 Hematologic and hematopoietic diseases / 002B19C Platelet diseases and coagulopathies
- Discipline
- Blood diseases
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4727010
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
10.1016/0140-6736(93)91070-3 
https://dx.doi.org/10.1016/0140-6736(93)91070-3
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