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Severe factor X deficiency in a pair of siblings: clinical presentation, phenotypic and genotypic features, prenatal diagnosis and treatment

✍ Scribed by J. INGERSLEV; T. HERLIN; B. SØRENSEN; N. CLAUSEN; K. C. CHU; K. A. HIGH


Book ID
108772783
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
472 KB
Volume
13
Category
Article
ISSN
1351-8216

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