Muhamad, Y.K. and Fuziah, M.Z. and Rus Anida, A. and Sidek, M.Ros and Ramli, S.F. and Adam, N. and Isa, M.N. (2001) Detection Of Point Mutation (Pro30Leu) In Exon 1 Of The 21-Hydroxylase Gene(Cyp21) In Patient With Congenital Adrenal Hyperplasia Using Digoxygenin System . In: 13th National Biotechnology Seminar , 10-13th November 2001, Bayview Hotel Pulau Pinang .
Congenital adrenal hyperplasia IS an autosomal recessive disease with a wide range of clinical manifestations.
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