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Pediatric Neurology
|
May 18, 1999
Neonatal type of nonketotic hyperglycinemia
F L Lu, P J Wang, W L Hwu, et al.
Clinical Genetics
|
March 29, 2000
Identification and characterization of -3c-g acceptor splice site mutation in human alpha-L-iduronidase associated with mucopolysaccharidosis type IH/S
Y N Teng, T R Wang, W L Hwu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
August 13, 1998
Human alpha-L-iduronidase (IDUA) gene: apparent recombination in intron 2 by haplotype analysis in a Taiwanese population
G J Lee-Chen, T R Wang, W L Hwu, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui
|
September 1, 1996
Camptomelic dysplasia: report of one case
P N Tsao, R J Teng, W L Hwu, et al.
Brain & Development
|
December 5, 1998
The controversy regarding diagnostic criteria for early myoclonic encephalopathy
P J Wang, W T Lee, W L Hwu, et al.
Clinical Genetics
|
September 15, 2017
Management of Leigh syndrome: Current status and new insights
L Chen, Y Cui, D Jiang, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
April 19, 2000
Late-onset holocarboxylase synthetase deficiency with homologous R508W mutation
W L Hwu, Y Suzuki, X Yang, et al.
Clinical Genetics
|
April 16, 2003
Two novel mutations in the alpha-galactosidase A gene in Chinese patients with Fabry disease
C-C Yang, L-W Lai, O Whitehair, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
June 28, 2000
Metabolic disorders mimicking Reye's syndrome
P F Chang, S F Huang, W L Hwu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
February 1, 1996
Hepatoblastoma in an infant with Beckwith-Wiedemann Syndrome
S Y Tsai, Y M Jeng, W L Hwu, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 77) with videos related to
Sort By:
Page
of 8
Pediatric Neurology
|
May 18, 1999
Neonatal type of nonketotic hyperglycinemia
F L Lu, P J Wang, W L Hwu, et al.
Clinical Genetics
|
March 29, 2000
Identification and characterization of -3c-g acceptor splice site mutation in human alpha-L-iduronidase associated with mucopolysaccharidosis type IH/S
Y N Teng, T R Wang, W L Hwu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
August 13, 1998
Human alpha-L-iduronidase (IDUA) gene: apparent recombination in intron 2 by haplotype analysis in a Taiwanese population
G J Lee-Chen, T R Wang, W L Hwu, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui
|
September 1, 1996
Camptomelic dysplasia: report of one case
P N Tsao, R J Teng, W L Hwu, et al.
Brain & Development
|
December 5, 1998
The controversy regarding diagnostic criteria for early myoclonic encephalopathy
P J Wang, W T Lee, W L Hwu, et al.
Clinical Genetics
|
September 15, 2017
Management of Leigh syndrome: Current status and new insights
L Chen, Y Cui, D Jiang, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
April 19, 2000
Late-onset holocarboxylase synthetase deficiency with homologous R508W mutation
W L Hwu, Y Suzuki, X Yang, et al.
Clinical Genetics
|
April 16, 2003
Two novel mutations in the alpha-galactosidase A gene in Chinese patients with Fabry disease
C-C Yang, L-W Lai, O Whitehair, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
June 28, 2000
Metabolic disorders mimicking Reye's syndrome
P F Chang, S F Huang, W L Hwu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
February 1, 1996
Hepatoblastoma in an infant with Beckwith-Wiedemann Syndrome
S Y Tsai, Y M Jeng, W L Hwu, et al.
Page
of 8