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Severe factor X deficiency in a pair of siblings: clinical presentation, phenotypic and genotypic features, prenatal diagnosis and treatment
Author(s) -
INGERSLEV J.,
HERLIN T.,
SØRENSEN B.,
CLAUSEN N.,
CHU K. C.,
HIGH K. A.
Publication year - 2007
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/j.1365-2516.2007.01466.x
Subject(s) - haemophilia , medicine , pediatrics , university hospital , haemophilia a , presentation (obstetrics) , family medicine , surgery