Pages that link to "Q45872903"
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The following pages link to Computational and molecular approaches for predicting unreported causal missense mutations in Belgian patients with haemophilia A. (Q45872903):
Displayed 6 items.
- Comprehensive analysis of phenotypes and genetics in 21 Chinese families with haemophilia B: characterization of five novel mutations. (Q30367118) (← links)
- Intron 22 homologous regions are implicated in exons 1-22 duplications of the F8 gene (Q37102092) (← links)
- Detection of new mutations and molecular pathology of mild and moderate haemophilia A patients from southern Brazil (Q43493283) (← links)
- Spectrum of Molecular Defects in 216 Chinese Families With Hemophilia A: Identification of Noninversion Mutation Hot Spots and 42 Novel Mutations. (Q45863386) (← links)
- Molecular diagnosis of haemophilia A in patients from Senegal. (Q45865764) (← links)
- Tandem inversion duplication within F8 Intron 1 associated with mild haemophilia A. (Q45875868) (← links)