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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 markerT R Wang, W L Hwu, J W Hou, et al.Journal of Biomedical Science|March 1, 1994
Cytogenetic Study of Mentally Retarded Children in TaipeiS. 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 caseW 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|January 1, 1996
Oculomotor apraxia in a case of Gaucher's disease with homozygous T1448C mutationL 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 caseF J Tsai, C T Peng, C H Tsai, 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 IIIBS 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 diseaseP J Wang, W L Hwu, W T Lee, et al.Pediatric Neurology|May 18, 1999
Neonatal type of nonketotic hyperglycinemiaF 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/SY 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 populationG J Lee-Chen, T R Wang, W L Hwu, et al.Pageof 17