Prenatal diagnosis in combined antithrombin and factor V gene mutation
- Author
- LANE, D. A1 ; AUBERGER, K2 ; IRELAND, H1 ; ROSCHER, A. A2 ; SWEE LAY THEIN3
[1] Charing Cross and Westminster Medical School, London, United Kingdom
[2] Dr von Haunersches Kinderspital, LMU München, München, Germany
[3] MRC Molecular Haematology Unit, Institute of Molecular Medicine, John Radcliffe Hospital, Oxford, United Kingdom - Source
British journal of haematology. 1996, Vol 94, Num 4, pp 753-755 ; ref : 12 ref
- CODEN
- BJHEAL
- ISSN
- 0007-1048
- Scientific domain
- Medical oncology; Hematology
- Publisher
- Blackwell, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Anticoagulant Antithrombine Diagnostic Déficit Etude cas Foetus Gène Homme Mutation Proaccélérine Prénatal Coagulopathie Foetus pathologie Gestation pathologie Hémopathie Maladie héréditaire
- Keyword (en)
- Anticoagulant Antithrombin Diagnosis Deficiency Case study Fetus Gene Human Mutation Factor V Prenatal Coagulopathy Fetal diseases Pregnancy disorders Hemopathy Genetic disease
- Keyword (es)
- Anticoagulante Antitrombina Diagnóstico Déficiencia Estudio caso Feto Gen Hombre Mutación Proacelerina Prenatal Coagulopatía Feto patología Gestación patología Hemopatía Enfermedad hereditaria
- 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
- 3209447
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
10.1046/j.1365-2141.1996.02347.x 
https://dx.doi.org/10.1046/j.1365-2141.1996.02347.x
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