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Showing items 51-61 of 61  (3 Page(s) Totally)
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Institution Date Title Author
亞洲大學 2003-05 Genetic analysis of chromosome 22q11.2 markers in congenital heart disease Shi YR;Hsieh KS;Wu,Jer-Yuarn;Lee,Chun-Cheng;YU MT;Jeng-Sheng Chang;Fuu-Jen Tsai;Chang-Hai Tsai
亞洲大學 2002-02 Monitoring of congenital adrenal hyperplasia by microbore HPLC-electrospray ionization tandem mass spectrometry of dried blood spots Lai,Chien-Chen;Tsai,Fuu-Jen;Wu,Jer-Yuarn;Wei-De Lin;Lee,Chun-Cheng;Chang-Hai Tsai
亞洲大學 2002-01 Rapid screening assay of congenital adrenal hyperplasia by measuring 17 alpha-hydroxyprogesterone with high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots Lai,Chien-Chen;Chang-Hai Tsai;Tsai,Fuu-Jen;Wu,Jer-Yuarn;Wei-De Lin;Lee,Chun-Cheng
亞洲大學 2002-01 Molecular analysis of syndromic congenital heart disease using short tandem repeat markers and semiquantitative polymerase chain reaction method Shi YR;Hsieh KS;Wu,Jer-Yuarn;Cheng-Chun Lee;Chang-Hai Tsai;Fuu-Jen Tsai
亞洲大學 2002 Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan Shi YR;Wu,Jer-Yuarn;Hsu YA;Cheng-Chun Lee;Chang-Hai Tsai;Fuu-Jen Tsai
亞洲大學 2001-12 Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation Wei-De Lin;Wu,Jer-Yuarn;Tsai,Fuu-Jen;Lee,Chun-Cheng;Chang-Hai Tsai
亞洲大學 2001-11 Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots Lai,Chien-Chen;Chang-Hai Tsai;Tsai,Fuu-Jen;Wu,Jer-Yuarn;Wei-De Lin;Lee,Chun-Cheng
亞洲大學 2001-07 A pilot study of neonatal screening by electrospray ionization tandem mass spectrometry in Taiwan Wei-De Lin;Wu,Jer-Yuarn;Lai,Chien-Chen;Tsai,Fuu-Jen;Chang-Hai Tsai
亞洲大學 2001-05 Pitfalls of PCR-based genotyping in patients with 21-hydroxylase deficiency Chang-Hai Tsai;Wei-De Lin;Tsai,Fuu-Jen;Peng,Ching-Tien;Wu,Jer-Yuarn
亞洲大學 2001 Relation of polymorphism in the region of human osteocalcin gene to bone mineral density and occurrence of osteoporosis in postmenopausal Chinese women in Taiwan Huey-Yi Chen;Tsai HD;Chen Wen-Chi;Wu,Jer-Yuarn;Fuu-Jen Tsai;Chang-Hai Tsai
亞洲大學 2000-10 A stop codon mutation in the CBFA 1 gene causes cleidocranial dysplasia Tsai,Fuu-Jen;Wu,Jer-Yuarn;Wei-De Lin;Chang-Hai Tsai

Showing items 51-61 of 61  (3 Page(s) Totally)
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