Authors:
Wu, CH
Hwu, WL
Wang, JK
Young, C
Peng, SSF
Kuo, MF
Citation: Ch. Wu et al., Deletion of 11q24.2-qter with agenesis of unilateral internal carotid artery and total anomalous pulmonary venous return, AM J MED G, 103(3), 2001, pp. 245-248
Authors:
Binzak, BA
Wevers, RA
Moolenaar, SH
Lee, YM
Hwu, WL
Poggi-Bach, J
Engelki, UFH
Hoard, HM
Vockley, JG
Vockley, J
Citation: Ba. Binzak et al., Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiency, AM J HU GEN, 68(4), 2001, pp. 839-847
Citation: Sc. Chiang et al., Glucose-6-phosphatase gene mutations in Taiwan Chinese patients with glycogen storage disease type Ia, J HUM GENET, 45(4), 2000, pp. 197-199
Citation: Yn. Teng et al., Identification and characterization of-3c-g acceptor splice site mutation in human alpha-L-iduronidase associated with mucopolysaccharidosis type IH/S, CLIN GENET, 57(2), 2000, pp. 131-136
Authors:
Ko, TM
Hwu, WL
Lin, YW
Tseng, LH
Hwa, HL
Wang, TR
Chuang, SM
Citation: Tm. Ko et al., Molecular genetic study of pompe disease in Chinese patients in Taiwan (vol 13, pg 380, 1998), HUM MUTAT, 14(1), 1999, pp. 86-86
Authors:
Hsu, YS
Hwu, WL
Huang, SF
Lu, MY
Chen, RL
Lin, DT
Peng, SSF
Lin, KH
Citation: Ys. Hsu et al., Niemann-Pick disease type C (a cellular cholesterol lipidosis) treated by bone marrow transplantation, BONE MAR TR, 24(1), 1999, pp. 103-107
Citation: Wl. Hwu et al., Hypercalcaemia in glycogen storage disease type Ia: A case with R83H and 341delG mutations, J INH MET D, 22(8), 1999, pp. 937-938