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.
| Main Authors: | , , , , , , |
|---|---|
| Format: | Conference or Workshop Item |
| Language: | English |
| Published: |
2001
|
| Subjects: | |
| 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 |
| _version_ | 1825828155258044416 |
|---|---|
| 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. |
| collection | USM |
| description | Congenital adrenal hyperplasia IS an autosomal recessive disease with a wide range of clinical manifestations. |
| first_indexed | 2024-03-06T13:49:23Z |
| format | Conference or Workshop Item |
| id | usm.eprints-7245 |
| institution | Universiti Sains Malaysia |
| language | English |
| last_indexed | 2024-03-06T13:49:23Z |
| publishDate | 2001 |
| record_format | dspace |
| spelling | usm.eprints-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/7245/1/Detection_of_point_mutation_%28pro30Leu%29_in_exon_1_of_the_21-hydroxylase_gene_%28CYP21%29_in_pattient_with_congenital_adrenal_hyperplasia_using.pdf |
| work_keys_str_mv | AT muhamadyk detectionofpointmutationpro30leuinexon1ofthe21hydroxylasegenecyp21inpatientwithcongenitaladrenalhyperplasiausingdigoxygeninsystem AT fuziahmz detectionofpointmutationpro30leuinexon1ofthe21hydroxylasegenecyp21inpatientwithcongenitaladrenalhyperplasiausingdigoxygeninsystem AT rusanidaa detectionofpointmutationpro30leuinexon1ofthe21hydroxylasegenecyp21inpatientwithcongenitaladrenalhyperplasiausingdigoxygeninsystem AT sidekmros detectionofpointmutationpro30leuinexon1ofthe21hydroxylasegenecyp21inpatientwithcongenitaladrenalhyperplasiausingdigoxygeninsystem AT ramlisf detectionofpointmutationpro30leuinexon1ofthe21hydroxylasegenecyp21inpatientwithcongenitaladrenalhyperplasiausingdigoxygeninsystem AT adamn detectionofpointmutationpro30leuinexon1ofthe21hydroxylasegenecyp21inpatientwithcongenitaladrenalhyperplasiausingdigoxygeninsystem AT isamn detectionofpointmutationpro30leuinexon1ofthe21hydroxylasegenecyp21inpatientwithcongenitaladrenalhyperplasiausingdigoxygeninsystem |