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T R Wang

Showing results (121-130 of 157) with videos related to

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Journal of the Formosan Medical Association = Taiwan Yi Zhi|February 1, 1996
Hepatoblastoma in an infant with Beckwith-Wiedemann SyndromeS Y Tsai, Y M Jeng, W L Hwu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|June 1, 1992
Familial nephrogenic diabetes insipidus: report of two familiesJ S Lee, W Y Tsai, W S Tsai, et al.
Zhonghua Minguo Wei Sheng Wu Ji Mian Yi Xue Za Zhi = Chinese Journal of Microbiology and Immunology|March 1, 1980
[Common variable immunodeficiency: an immunological study (author's transl)]K S Tsai, C Y Chuang, K H Hsieh, et al.
Human Mutation|February 6, 1998
Two common mutations 934C to G and 937C to G of fibroblast growth factor receptor 2 (FGFR2) gene in Chinese patients with Apert syndromeF J Tsai, W L Hwu, S P Lin, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|July 27, 2000
Corneal opacity and congenital glaucoma associated with massive heparan sulfaturia: report of one caseS C Lin, F R Hu, J W Hou, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|June 1, 1994
Congenital nephrotic syndrome with microcephaly: report of a caseC H Yu, W S Tsai, P J Wang, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|February 1, 1993
Cardiovascular disorders in Turner's syndrome and its correlation to karyotypeJ W Hou, W L Hwu, W Y Tsai, et al.
Journal of Human Genetics|August 17, 2000
Glucose-6-phosphatase gene mutations in Taiwan Chinese patients with glycogen storage disease type IaS C Chiang, Y M Lee, M H Chang, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|August 6, 2000
Congenital contractural arachnodactyly (Beals syndrome)P H Su, J W Hou, W L Hwu, et al.
Human Genetics|February 1, 1996
Arylsulfatase A pseudodeficiency in ChineseW L Hwu, L P Tsai, W C Wang, et al.
Pageof 16

Showing results (121-130 of 157) with videos related to

Sort By:
Pageof 16
Journal of the Formosan Medical Association = Taiwan Yi Zhi|February 1, 1996
Hepatoblastoma in an infant with Beckwith-Wiedemann SyndromeS Y Tsai, Y M Jeng, W L Hwu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|June 1, 1992
Familial nephrogenic diabetes insipidus: report of two familiesJ S Lee, W Y Tsai, W S Tsai, et al.
Zhonghua Minguo Wei Sheng Wu Ji Mian Yi Xue Za Zhi = Chinese Journal of Microbiology and Immunology|March 1, 1980
[Common variable immunodeficiency: an immunological study (author's transl)]K S Tsai, C Y Chuang, K H Hsieh, et al.
Human Mutation|February 6, 1998
Two common mutations 934C to G and 937C to G of fibroblast growth factor receptor 2 (FGFR2) gene in Chinese patients with Apert syndromeF J Tsai, W L Hwu, S P Lin, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|July 27, 2000
Corneal opacity and congenital glaucoma associated with massive heparan sulfaturia: report of one caseS C Lin, F R Hu, J W Hou, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|June 1, 1994
Congenital nephrotic syndrome with microcephaly: report of a caseC H Yu, W S Tsai, P J Wang, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|February 1, 1993
Cardiovascular disorders in Turner's syndrome and its correlation to karyotypeJ W Hou, W L Hwu, W Y Tsai, et al.
Journal of Human Genetics|August 17, 2000
Glucose-6-phosphatase gene mutations in Taiwan Chinese patients with glycogen storage disease type IaS C Chiang, Y M Lee, M H Chang, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|August 6, 2000
Congenital contractural arachnodactyly (Beals syndrome)P H Su, J W Hou, W L Hwu, et al.
Human Genetics|February 1, 1996
Arylsulfatase A pseudodeficiency in ChineseW L Hwu, L P Tsai, W C Wang, et al.
Pageof 16