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Human Mutation
|
February 6, 1998
Possible common mutations in the low density lipoprotein receptor gene in Chinese
Y T Mak, J Zhang, Y S Chan, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
October 9, 1998
Mutations in the low-density lipoprotein receptor gene in Chinese familial hypercholesterolemia patients
Y T Mak, C P Pang, B Tomlinson, et al.
Eye (London, England)
|
July 12, 2008
A novel mutation in CRYBB2 responsible for inherited coronary cataract
D Lou, J-P Tong, L-Y Zhang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 5, 1998
Rarity of debrisoquine hydroxylase gene polymorphism in Chinese patients with Parkinson's disease
C P Pang, J Zhang, J Woo, et al.
Journal of Inherited Metabolic Disease
|
March 1, 1997
An unusual case of multiple carboxylase deficiency presenting as generalized pustular psoriasis in a Chinese boy
L K Law, C Y Lau, C P Pang, et al.
The Biochemical Journal
|
September 15, 1984
Stereochemistry of the incorporation of valine methyl groups into methylene groups in cephalosporin C
C P Pang, R L White, E P Abraham, et al.
Investigative Ophthalmology & Visual Science
|
May 8, 2000
Truncations in the TIGR gene in individuals with and without primary open-angle glaucoma
D S Lam, Y F Leung, J K Chua, et al.
The British Journal of Ophthalmology
|
August 25, 2001
Rhodopsin mutations in Chinese patients with retinitis pigmentosa
W M Chan, K Y Yeung, C P Pang, et al.
Eye (London, England)
|
March 15, 2006
An in vitro study on the compatibility and concentrations of combinations of vancomycin, amikacin, and dexamethasone in human vitreous
M Hui, A K H Kwok, C P Pang, et al.
Archives of Neurology
|
April 18, 2000
The alpha-synuclein gene and Parkinson disease in a Chinese population
D K Chan, G Mellick, H Cai, et al.
Page
of 14
Search research articles
Search
Showing results (71-80 of 132) with videos related to
Sort By:
Page
of 14
Human Mutation
|
February 6, 1998
Possible common mutations in the low density lipoprotein receptor gene in Chinese
Y T Mak, J Zhang, Y S Chan, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
October 9, 1998
Mutations in the low-density lipoprotein receptor gene in Chinese familial hypercholesterolemia patients
Y T Mak, C P Pang, B Tomlinson, et al.
Eye (London, England)
|
July 12, 2008
A novel mutation in CRYBB2 responsible for inherited coronary cataract
D Lou, J-P Tong, L-Y Zhang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 5, 1998
Rarity of debrisoquine hydroxylase gene polymorphism in Chinese patients with Parkinson's disease
C P Pang, J Zhang, J Woo, et al.
Journal of Inherited Metabolic Disease
|
March 1, 1997
An unusual case of multiple carboxylase deficiency presenting as generalized pustular psoriasis in a Chinese boy
L K Law, C Y Lau, C P Pang, et al.
The Biochemical Journal
|
September 15, 1984
Stereochemistry of the incorporation of valine methyl groups into methylene groups in cephalosporin C
C P Pang, R L White, E P Abraham, et al.
Investigative Ophthalmology & Visual Science
|
May 8, 2000
Truncations in the TIGR gene in individuals with and without primary open-angle glaucoma
D S Lam, Y F Leung, J K Chua, et al.
The British Journal of Ophthalmology
|
August 25, 2001
Rhodopsin mutations in Chinese patients with retinitis pigmentosa
W M Chan, K Y Yeung, C P Pang, et al.
Eye (London, England)
|
March 15, 2006
An in vitro study on the compatibility and concentrations of combinations of vancomycin, amikacin, and dexamethasone in human vitreous
M Hui, A K H Kwok, C P Pang, et al.
Archives of Neurology
|
April 18, 2000
The alpha-synuclein gene and Parkinson disease in a Chinese population
D K Chan, G Mellick, H Cai, et al.
Page
of 14