Hemophilia
Novel genetic hemophilia markers improve prenatal diagnosis
Published in Cancer Weekly, September 2nd, 2003
"The heterogeneous nature of the mutations, the size, and the complexity of the factor VIII gene makes direct mutation analysis in hemophilia A families in India an option that is not very feasible and practical," scientists in New Delhi explained. "Thus, carrier screening and prenatal diagnosis of hemophilia A often depends on haplotype analysis using restriction fragment length polymorphisms (RFLP) and short tandem repeat (STR) markers to track the defective factor VIII gene within a family."
M.R. Chowdhury and colleagues at the All India Institute of Medical Sciences...
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Source: Cancer Weekly (2003-09-02)
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