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机构 日期 题名 作者
臺大學術典藏 2020-06-27T06:40:11Z DiGeorge sequence with hypogammaglobulinemia: A case report Kuo P.-L.; BOR-LUEN CHIANG; Hwu W.-L.; Chien Y.-H.;Yang Y.-H.;Chu S.-Y.;Hwu W.-L.;Kuo P.-L.;Bor-Luen Chiang; Chien Y.-H.; Yang Y.-H.; Chu S.-Y.
臺大學術典藏 2020-06-27T06:40:09Z Common variable immunodeficiency with hypoglycemia, Kikuchi lymphadenitis, and hemiparesis in two siblings Chien Y.-H.;Yang Y.-H.;Hwu W.-L.;Chou C.-C.;Bor-Luen Chiang; Chien Y.-H.; Yang Y.-H.; Hwu W.-L.; Chou C.-C.; BOR-LUEN CHIANG
臺大學術典藏 2020-06-27T06:40:01Z Molecular diagnosis of Wiskott-Aldrich syndrome in Taiwan Chien Y.-H.;Hwu W.-L.;Ariga T.;Chang K.-W.;Yang Y.-H.;Lin K.-H.;Bor-Luen Chiang; Chien Y.-H.; Hwu W.-L.; Ariga T.; Chang K.-W.; Yang Y.-H.; Lin K.-H.; BOR-LUEN CHIANG
臺大學術典藏 2020-06-27T06:39:43Z The genetics of atopic dermatitis Chien Y.-H.;Hwu W.-L.;Bor-Luen Chiang; Chien Y.-H.; Hwu W.-L.; BOR-LUEN CHIANG
臺大學術典藏 2020-06-27T06:39:24Z Distribution, clinical features and treatment in Taiwanese patients with symptomatic primary immunodeficiency diseases (PIDs) in a nationwide population-based study during 1985-2010 Lee W.-I.;Huang J.-L.;Jaing T.-H.;Shyur S.-D.;Yang K.D.;Chien Y.-H.;Bor-Luen Chiang;Soong W.-J.;Chiou S.-S.;Shieh C.-C.;Lin S.-J.;Yeh K.-W.;Chen L.-C.;Ou L.-S.;Yao T.-C.;Lin T.-Y.;Chiu C.-H.;Huang Y.-C.;Wu K.-H.;Lin C.-Y.;Yu H.-H.;Yang Y.-H.;Yu H.-R.;Yen H.-J.;Hsieh M.-Y.;Kuo M.-L.;Hwu W.-L.;Tsai Y.-C.;Kuo H.-C.;Lin Y.-L.;Shih Y.-F.;Chang K.-W.; Lee W.-I.; Huang J.-L.; Jaing T.-H.; Shyur S.-D.; Yang K.D.; Chien Y.-H.; BOR-LUEN CHIANG; Soong W.-J.; Chiou S.-S.; Shieh C.-C.; Lin S.-J.; Yeh K.-W.; Chen L.-C.; Ou L.-S.; Yao T.-C.; Lin T.-Y.; Chiu C.-H.; Huang Y.-C.; Wu K.-H.; Lin C.-Y.; Yu H.-H.; Yang Y.-H.; Yu H.-R.; Yen H.-J.; Hsieh M.-Y.; Kuo M.-L.; Hwu W.-L.; Tsai Y.-C.; Kuo H.-C.; Lin Y.-L.; Shih Y.-F.; Chang K.-W.
臺大學術典藏 2020-06-27T06:38:52Z Mycobacterium abscessus infection in a boy with X-linked anhidrotic ectodermal dysplasia, immunodeficiency Yu H.-H.;Hu T.-C.;Lee N.-C.;Chien Y.-H.;Yang Y.-H.;Hwu W.-L.;Bor-Luen Chiang; Yu H.-H.; Hu T.-C.; Lee N.-C.; Chien Y.-H.; Yang Y.-H.; Hwu W.-L.; BOR-LUEN CHIANG
臺大學術典藏 2020-05-25T06:51:59Z Multimodel assessment of BRCA1 mutations in Taiwanese (ethnic Chinese) women with early-onset, bilateral or familial breast cancer Chang K.-J.;Hwu W.-L;Hsieh F.-J;Cheng A.-L;Lin C.-H;Sargeant A.M;Bai L.-Y;Yen-Shen Lu;Liu T.-P;Chien Y.-H;Huang A.-C;Lin P.-H;Kuo W.-H; Kuo W.-H; Lin P.-H; Huang A.-C; Chien Y.-H; Liu T.-P; YEN-SHEN LU; Bai L.-Y; Sargeant A.M; Lin C.-H; Cheng A.-L; Hsieh F.-J; Hwu W.-L; Chang K.-J.
臺大學術典藏 2020-04-24T01:34:25Z Phenotypic analyses and mutation screening of the SLC26A4 and FOXI1 genes in 101 Taiwanese families with bilateral nonsyndromic enlarged vestibular aqueduct (DFNB4) or pendred syndrome Hsu C.-J.; Hwu W.-L.; Su Y.-N.; Yeh P.-L.; Chen P.-J.; Lu Y.-C.; Chen-Chi Wu
臺大學術典藏 2020-04-24T01:34:25Z Application of SNaPshot multiplex assays for simultaneous multigene mutation screening in patients with idiopathic sensorineural hearing impairment Chen-Chi Wu; Lu Y.-C.; Chen P.-J.; Liu A.Y.-Z.; Hwu W.-L.; Hsu C.-J.
臺大學術典藏 2020-04-24T01:34:23Z Mutation screening of the EYA1, SIX1, and SIX5 genes in an East Asian cohort with branchio-oto-renal syndrome Wang S.-H.; Chen-Chi Wu; Lu Y.-C.; Lin Y.-H.; Su Y.-N.; Hwu W.-L.; Yu I.-S.; Hsu C.-J.

显示项目 531-540 / 770 (共77页)
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