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Analytical Biochemistry
|
March 31, 2009
Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis
Chia-Cheng Hung, Shin-Yu Lin, Chien-Nan Lee, et al.
Journal of Inherited Metabolic Disease
|
September 8, 2010
Enzyme assay and clinical assessment in subjects with a Chinese hotspot late-onset Fabry mutation (IVS4 + 919G→A)
Hsiang-Yu Lin, Cheng-Hung Huang, Hsiao-Chi Yu, et al.
Molecular Genetics and Metabolism Reports
|
May 3, 2016
Long-term galsulfase enzyme replacement therapy in Taiwanese mucopolysaccharidosis VI patients: A case series
Hsiang-Yu Lin, Chih-Kuang Chuang, Chung-Hsing Wang, et al.
American Journal of Medical Genetics. Part A
|
March 11, 2006
Clinical characteristics and survival of trisomy 18 in a medical center in Taipei, 1988-2004
Hsiang-Yu Lin, Shuan-Pei Lin, Yen-Jiun Chen, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
May 30, 2007
Clinical characteristics and survival of trisomy 13 in a medical center in Taiwan, 1985-2004
Hsiang-Yu Lin, Shuan-Pei Lin, Yen-Jiun Chen, et al.
Biochemical Genetics
|
May 28, 2014
Two frequent mutations associated with the classic form of propionic acidemia in Taiwan
Yen-Hui Chiu, Yu-Ning Liu, Wei-Ling Liao, et al.
The Journal of Pediatrics
|
November 10, 2018
Taiwan National Newborn Screening Program by Tandem Mass Spectrometry for Mucopolysaccharidoses Types I, II, and VI
Min-Ju Chan, Hsuan-Chieh Liao, Michael H Gelb, et al.
Diagnostics (Basel, Switzerland)
|
September 28, 2021
Nationwide Newborn Screening Program for Mucopolysaccharidoses in Taiwan and an Update of the "Gold Standard" Criteria Required to Make a Confirmatory Diagnosis
Chih-Kuang Chuang, Chung-Lin Lee, Ru-Yi Tu, et al.
Journal of Clinical Immunology
|
May 16, 2008
Genetic polymorphisms in the CD40 ligand gene and Kawasaki disease
Fu-Yuan Huang, Tzu-Yang Chang, Ming-Ren Chen, et al.
American Journal of Medical Genetics. Part A
|
April 27, 2018
Functional independence of Taiwanese children with Prader-Willi syndrome
Chung-Lin Lee, Hsiang-Yu Lin, Li-Ping Tsai, et al.
Page
of 29
Search research articles
Search
Showing results (231-240 of 281) with videos related to
Sort By:
Page
of 29
Analytical Biochemistry
|
March 31, 2009
Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis
Chia-Cheng Hung, Shin-Yu Lin, Chien-Nan Lee, et al.
Journal of Inherited Metabolic Disease
|
September 8, 2010
Enzyme assay and clinical assessment in subjects with a Chinese hotspot late-onset Fabry mutation (IVS4 + 919G→A)
Hsiang-Yu Lin, Cheng-Hung Huang, Hsiao-Chi Yu, et al.
Molecular Genetics and Metabolism Reports
|
May 3, 2016
Long-term galsulfase enzyme replacement therapy in Taiwanese mucopolysaccharidosis VI patients: A case series
Hsiang-Yu Lin, Chih-Kuang Chuang, Chung-Hsing Wang, et al.
American Journal of Medical Genetics. Part A
|
March 11, 2006
Clinical characteristics and survival of trisomy 18 in a medical center in Taipei, 1988-2004
Hsiang-Yu Lin, Shuan-Pei Lin, Yen-Jiun Chen, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
May 30, 2007
Clinical characteristics and survival of trisomy 13 in a medical center in Taiwan, 1985-2004
Hsiang-Yu Lin, Shuan-Pei Lin, Yen-Jiun Chen, et al.
Biochemical Genetics
|
May 28, 2014
Two frequent mutations associated with the classic form of propionic acidemia in Taiwan
Yen-Hui Chiu, Yu-Ning Liu, Wei-Ling Liao, et al.
The Journal of Pediatrics
|
November 10, 2018
Taiwan National Newborn Screening Program by Tandem Mass Spectrometry for Mucopolysaccharidoses Types I, II, and VI
Min-Ju Chan, Hsuan-Chieh Liao, Michael H Gelb, et al.
Diagnostics (Basel, Switzerland)
|
September 28, 2021
Nationwide Newborn Screening Program for Mucopolysaccharidoses in Taiwan and an Update of the "Gold Standard" Criteria Required to Make a Confirmatory Diagnosis
Chih-Kuang Chuang, Chung-Lin Lee, Ru-Yi Tu, et al.
Journal of Clinical Immunology
|
May 16, 2008
Genetic polymorphisms in the CD40 ligand gene and Kawasaki disease
Fu-Yuan Huang, Tzu-Yang Chang, Ming-Ren Chen, et al.
American Journal of Medical Genetics. Part A
|
April 27, 2018
Functional independence of Taiwanese children with Prader-Willi syndrome
Chung-Lin Lee, Hsiang-Yu Lin, Li-Ping Tsai, et al.
Page
of 29