Detection Of Point Mutation (Pro30Leu) In Exon 1 Of The 21-Hydroxylase Gene(Cyp21) In Patient With Congenital Adrenal Hyperplasia Using Digoxygenin System .

Congenital adrenal hyperplasia IS an autosomal recessive disease with a wide range of clinical manifestations.

Bibliographic Details
Main Authors:	Muhamad, Y.K., Fuziah, M.Z., Rus Anida, A., Sidek, M.Ros, Ramli, S.F., Adam, N., Isa, M.N.
Format:	Conference or Workshop Item
Language:	English
Published:	2001
Subjects:	R5-920 Medicine (General)
Online Access:	http://eprints.usm.my/7245/ http://eprints.usm.my/7245/1/Detection_of_point_mutation_%28pro30Leu%29_in_exon_1_of_the_21-hydroxylase_gene_%28CYP21%29_in_pattient_with_congenital_adrenal_hyperplasia_using.pdf

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author	Muhamad, Y.K. Fuziah, M.Z. Rus Anida, A. Sidek, M.Ros Ramli, S.F. Adam, N. Isa, M.N.
author_facet	Muhamad, Y.K. Fuziah, M.Z. Rus Anida, A. Sidek, M.Ros Ramli, S.F. Adam, N. Isa, M.N.
author_sort	Muhamad, Y.K.
building	USM Institutional Repository
collection	Online Access
description	Congenital adrenal hyperplasia IS an autosomal recessive disease with a wide range of clinical manifestations.
first_indexed	2025-11-15T15:20:20Z
format	Conference or Workshop Item
id	usm-7245
institution	Universiti Sains Malaysia
institution_category	Local University
language	English
last_indexed	2025-11-15T15:20:20Z
publishDate	2001
recordtype	eprints
repository_type	Digital Repository
spelling	usm-72452013-07-13T03:37:11Z http://eprints.usm.my/7245/ Detection Of Point Mutation (Pro30Leu) In Exon 1 Of The 21-Hydroxylase Gene(Cyp21) In Patient With Congenital Adrenal Hyperplasia Using Digoxygenin System . Muhamad, Y.K. Fuziah, M.Z. Rus Anida, A. Sidek, M.Ros Ramli, S.F. Adam, N. Isa, M.N. R5-920 Medicine (General) Congenital adrenal hyperplasia IS an autosomal recessive disease with a wide range of clinical manifestations. 2001-11 Conference or Workshop Item PeerReviewed application/pdf en http://eprints.usm.my/7245/1/Detection_of_point_mutation_%28pro30Leu%29_in_exon_1_of_the_21-hydroxylase_gene_%28CYP21%29_in_pattient_with_congenital_adrenal_hyperplasia_using.pdf 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 .
spellingShingle	R5-920 Medicine (General) Muhamad, Y.K. Fuziah, M.Z. Rus Anida, A. Sidek, M.Ros Ramli, S.F. Adam, N. Isa, M.N. Detection Of Point Mutation (Pro30Leu) In Exon 1 Of The 21-Hydroxylase Gene(Cyp21) In Patient With Congenital Adrenal Hyperplasia Using Digoxygenin System .
title	Detection Of Point Mutation (Pro30Leu) In Exon 1 Of The 21-Hydroxylase Gene(Cyp21) In Patient With Congenital Adrenal Hyperplasia Using Digoxygenin System .
title_full	Detection Of Point Mutation (Pro30Leu) In Exon 1 Of The 21-Hydroxylase Gene(Cyp21) In Patient With Congenital Adrenal Hyperplasia Using Digoxygenin System .
title_fullStr	Detection Of Point Mutation (Pro30Leu) In Exon 1 Of The 21-Hydroxylase Gene(Cyp21) In Patient With Congenital Adrenal Hyperplasia Using Digoxygenin System .
title_full_unstemmed	Detection Of Point Mutation (Pro30Leu) In Exon 1 Of The 21-Hydroxylase Gene(Cyp21) In Patient With Congenital Adrenal Hyperplasia Using Digoxygenin System .
title_short	Detection Of Point Mutation (Pro30Leu) In Exon 1 Of The 21-Hydroxylase Gene(Cyp21) In Patient With Congenital Adrenal Hyperplasia Using Digoxygenin System .
title_sort	detection of point mutation (pro30leu) in exon 1 of the 21-hydroxylase gene(cyp21) in patient with congenital adrenal hyperplasia using digoxygenin system .
topic	R5-920 Medicine (General)
url	http://eprints.usm.my/7245/ http://eprints.usm.my/7245/1/Detection_of_point_mutation_%28pro30Leu%29_in_exon_1_of_the_21-hydroxylase_gene_%28CYP21%29_in_pattient_with_congenital_adrenal_hyperplasia_using.pdf

Detection Of Point Mutation (Pro30Leu) In Exon 1 Of The 21-Hydroxylase Gene(Cyp21) In Patient With Congenital Adrenal Hyperplasia Using Digoxygenin System .

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