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Pediatric Neurology
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September 1, 1996
Homocystinuria presenting as fatal common carotid artery occlusion
C Y Lu, J W Hou, P J Wang, 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.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui
|
May 1, 1992
Marinesco-Sjögren syndrome: report of one case
Y H Chou, M Y Lin, P J Wang, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
January 28, 1998
Partial DiGeorge anomaly associated with 10p deletion
H L Hsu, P H Hsiao, J W Hou, et al.
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.
Journal of Pediatric Gastroenterology and Nutrition
|
March 1, 1987
Neonatal hepatitis: a follow-up study
M H Chang, H C Hsu, C Y Lee, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
January 1, 1993
Clinical characteristics of congenital hypothyroidism detected by neonatal screening
W Y Tsai, J S Lee, T R Wang, 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.
Page
of 16
Search research articles
Search
Showing results (91-100 of 157) with videos related to
Sort By:
Page
of 16
Pediatric Neurology
|
September 1, 1996
Homocystinuria presenting as fatal common carotid artery occlusion
C Y Lu, J W Hou, P J Wang, 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.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui
|
May 1, 1992
Marinesco-Sjögren syndrome: report of one case
Y H Chou, M Y Lin, P J Wang, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
January 28, 1998
Partial DiGeorge anomaly associated with 10p deletion
H L Hsu, P H Hsiao, J W Hou, et al.
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.
Journal of Pediatric Gastroenterology and Nutrition
|
March 1, 1987
Neonatal hepatitis: a follow-up study
M H Chang, H C Hsu, C Y Lee, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
January 1, 1993
Clinical characteristics of congenital hypothyroidism detected by neonatal screening
W Y Tsai, J S Lee, T R Wang, 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.
Page
of 16