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Segmental isodisomy and skewed X-inactivation resulting in haemophilia B in a female

✍ Scribed by L. N. Sellner; P. J. Price


Book ID
108673464
Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
111 KB
Volume
131
Category
Article
ISSN
0007-1048

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Hemophilia B in a female carrier due to
✍ Chan, Vivian; Chan, V. Wan Yin; Yip, Ben; Chim, C. S.; Chan, T. K. πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 234 KB πŸ‘ 2 views

A novel missense mutation (codon 351, GCT (Ala) β†’ CCT (Pro)) of the FIX gene was characterised in a young female with mild hemophilia B. She is heterozygous for the FIX mutation inherited from her carrier mother. Analysis of the methyl-sensitive Hpa II sites at the 5 end of the hypoxanthine phosphor