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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 caseP N Tsao, R J Teng, W L Hwu, et al.Journal of the Formosan Medical Association = Taiwan Yi Zhi|February 1, 1996
Hepatoblastoma in an infant with Beckwith-Wiedemann SyndromeS Y Tsai, Y M Jeng, W L Hwu, et al.Brain & Development|January 23, 2025
Newborn screening of neurometabolic diseases for early treatmentY-H Chien, W-L HwuZhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui|May 1, 1995
Sex determination in infants with ambiguous genitalia using the polymerase chain reaction of SRY geneF J Tsai, C H Tsai, W L Hwu, et al.Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui|July 1, 1991
Crisis in Gaucher disease simulating osteomyelitis: report of one caseY C Lai, W L Hwu, T R Wang, et al.Human Genetics|September 15, 2000
Dopa-responsive dystonia induced by a recessive GTP cyclohydrolase I mutationW L Hwu, P J Wang, K J Hsiao, et al.Journal of the Formosan Medical Association = Taiwan Yi Zhi|February 1, 1993
Cardiovascular disorders in Turner's syndrome and its correlation to karyotypeJ W Hou, W L Hwu, W Y Tsai, et al.Journal of Human Genetics|August 17, 2000
Glucose-6-phosphatase gene mutations in Taiwan Chinese patients with glycogen storage disease type IaS C Chiang, Y M Lee, M H Chang, et al.Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|August 6, 2000
Congenital contractural arachnodactyly (Beals syndrome)P H Su, J W Hou, W L Hwu, et al.Human Genetics|February 1, 1996
Arylsulfatase A pseudodeficiency in ChineseW L Hwu, L P Tsai, W C Wang, et al.Pageof 17