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Risk of erroneous results in carrier testing for haemophilia A without prior DNA analysis in male index patients
Author(s) -
Fransen van de Putte D. E.,
Frankhuizen W. S.,
Vijfhuizen L.,
Groenewegen L.,
Tamminga R. Y. J.,
Bouman K.,
Essen A. J.,
Gijsbers A. C. J.,
Ruivenkamp C. A. L.,
Boon E. M. J.
Publication year - 2015
Publication title -
haemophilia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.213
H-Index - 92
eISSN - 1365-2516
pISSN - 1351-8216
DOI - 10.1111/hae.12648
Subject(s) - medicine , medical genetics , center (category theory) , factor v leiden , pediatrics , genetics , biology , chemistry , thrombosis , gene , venous thrombosis , crystallography
D. E. FRANSEN VAN DE PUTTE,* W. S. FRANKHUIZEN,* L. VIJFHUIZEN,* L. GROENEWEGEN,* R. Y. J . TAMMINGA,† K. BOUMAN,‡ A. J . VAN ESSEN,‡ A. C. J . GIJSBERS,* C. A. L. RUIVENKAMP* and E. M. J . BOON* *Department of Clinical Genetics, Leiden University Medical Center, Leiden; †University Medical Center Groningen, Beatrix Children’s Hospital; and ‡Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands