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.

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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/7245/1/Detection_of_point_mutation_%28pro30Leu%29_in_exon_1_of_the_21-hydroxylase_gene_%28CYP21%29_in_pattient_with_congenital_adrenal_hyperplasia_using.pdf http://eprints.usm.my/7245/
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Institution:	Universiti Sains Malaysia
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spelling	my.usm.eprints.7245 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 .
institution	Universiti Sains Malaysia
building	Hamzah Sendut Library
collection	Institutional Repository
continent	Asia
country	Malaysia
content_provider	Universiti Sains Malaysia
content_source	USM Institutional Repository
url_provider	http://eprints.usm.my/
language	English
topic	R5-920 Medicine (General)
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 .
description	Congenital adrenal hyperplasia IS an autosomal recessive disease with a wide range of clinical manifestations.
format	Conference or Workshop Item
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.
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_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_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_sort	detection of point mutation (pro30leu) in exon 1 of the 21-hydroxylase gene(cyp21) in patient with congenital adrenal hyperplasia using digoxygenin system .
publishDate	2001
url	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 http://eprints.usm.my/7245/
_version_	1643700665349832704

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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