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Journal of Biomedical Science
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March 1, 1994
Cytogenetic Study of Mentally Retarded Children in Taipei
S. Wang-Wuu, Y.-M. Lai, W.-L. Hwu, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui
|
March 1, 1991
Prader-Willi syndrome with chromosome 15 interstitial deletion: report of one case
W L Hwu, W Y Tsai, J S Lee, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui
|
March 1, 1993
Fragile-X mental retardation--a combination of cytogenetic and molecular approaches, with greater emphasis on DNA analysis
T R Wang, W L Hwu, J W Hou, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui
|
March 1, 1993
Y-specific polymerase chain reaction for the interpretation of a chromosome marker
T R Wang, W L Hwu, J W Hou, et al.
Journal of Medical Virology
|
January 1, 1992
Transfusion-acquired cytomegalovirus infection in children in a hyperendemic area
P I Lee, M H Chang, W L Hwu, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui
|
January 1, 1996
Oculomotor apraxia in a case of Gaucher's disease with homozygous T1448C mutation
L P Tsai, W C Sue, W L Hwu, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui
|
May 1, 1991
Niemann-Pick disease type B with ocular involvement: report of a case
F J Tsai, C T Peng, C H Tsai, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi
|
October 6, 2000
Hereditary fructose intolerance presenting as Reye's-like syndrome: report of one case
T Y Yang, H L Chen, Y H Ni, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui
|
September 1, 1996
Diagnosis of mucopolysaccharidosis type IIIB
S C Chuang, W L Hwu, C C Wu, et al.
Pediatric Neurology
|
November 21, 1997
Duplication of proteolipid protein gene: a possible major cause of Pelizaeus-Merzbacher disease
P J Wang, W L Hwu, W T Lee, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 77) with videos related to
Sort By:
Page
of 8
Journal of Biomedical Science
|
March 1, 1994
Cytogenetic Study of Mentally Retarded Children in Taipei
S. Wang-Wuu, Y.-M. Lai, W.-L. Hwu, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui
|
March 1, 1991
Prader-Willi syndrome with chromosome 15 interstitial deletion: report of one case
W L Hwu, W Y Tsai, J S Lee, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui
|
March 1, 1993
Fragile-X mental retardation--a combination of cytogenetic and molecular approaches, with greater emphasis on DNA analysis
T R Wang, W L Hwu, J W Hou, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui
|
March 1, 1993
Y-specific polymerase chain reaction for the interpretation of a chromosome marker
T R Wang, W L Hwu, J W Hou, et al.
Journal of Medical Virology
|
January 1, 1992
Transfusion-acquired cytomegalovirus infection in children in a hyperendemic area
P I Lee, M H Chang, W L Hwu, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui
|
January 1, 1996
Oculomotor apraxia in a case of Gaucher's disease with homozygous T1448C mutation
L P Tsai, W C Sue, W L Hwu, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui
|
May 1, 1991
Niemann-Pick disease type B with ocular involvement: report of a case
F J Tsai, C T Peng, C H Tsai, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi
|
October 6, 2000
Hereditary fructose intolerance presenting as Reye's-like syndrome: report of one case
T Y Yang, H L Chen, Y H Ni, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui
|
September 1, 1996
Diagnosis of mucopolysaccharidosis type IIIB
S C Chuang, W L Hwu, C C Wu, et al.
Pediatric Neurology
|
November 21, 1997
Duplication of proteolipid protein gene: a possible major cause of Pelizaeus-Merzbacher disease
P J Wang, W L Hwu, W T Lee, et al.
Page
of 8