Mutations Of Pro30Leu And Val281Leu Of The Cyp21 Gene In Patients Diagnosed With Ambiguous Genitalia.
Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders of adrenal steroidogenesis.
Main Authors: | Isa, M.N., Muhamad, Y.K., Fuziah, M.Z., Rus Anida, A., Sidek, M.Ros, Ramli, S.F. |
---|---|
Format: | Conference or Workshop Item |
Language: | English |
Published: |
2002
|
Subjects: | |
Online Access: | http://eprints.usm.my/7185/1/Mutations_of_pro30Leu_and_Va1281_Leu_of_the_cyp21_gene_in_patients_diagnosed_with_ambiguous_genitalia.pdf |
Similar Items
-
Molecular Analysis In Gender Assignment And Management Of
Ambiguous Genitalia.
by: Muhamad, Y.K., et al.
Published: (2001) -
Detection Of Point Mutation (Pro30Leu) In Exon 1 Of The 21-Hydroxylase Gene(Cyp21) In Patient With Congenital
Adrenal Hyperplasia Using Digoxygenin System .
by: Muhamad, Y.K., et al.
Published: (2001) -
Molecular Analysis In The Management Of Congenital Adrenal Hyperplasia (CAH) And Ambiguous Genitalia.
by: Isa, M.N., et al.
Published: (2002) -
Molecular Analysis Of Cyp21 Gene In Patients Presenting With Ambiguous Genitalia.
by: Fuziah, M Z, et al.
Published: (2002) -
Molecular detection of genetic defects in ambiguous genitalia (AG) and congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency
by: Zain, Fuziah Md, et al.
Published: (2000)