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Zhonghua 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 gene
F 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 case
Y 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 mutation
W 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 karyotype
J 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 Ia
S 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 Chinese
W L Hwu, L P Tsai, W C Wang, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui
|
May 1, 1996
Sex determination in infants with ambiguous genitalia using the polymerase chain reaction of an X-Y homologous region
C H Tsai, F J Tsai, W L Hwu, et al.
Human Mutation
|
August 31, 2002
A founder mutation (R254X) of SLC22A5 (OCTN2) in Chinese primary carnitine deficiency patients
Nelson L S Tang, W L Hwu, Rachel T Chan, et al.
Journal of Inherited Metabolic Disease
|
August 19, 2007
Deficiency of the carnitine transporter (OCTN2) with partial N-acetylglutamate synthase (NAGS) deficiency
W-L Hwu, Y-H Chien, N L S Tang, et al.
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Showing results (41-50 of 77) with videos related to
Sort By:
Page
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Zhonghua 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 gene
F 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 case
Y 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 mutation
W 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 karyotype
J 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 Ia
S 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 Chinese
W L Hwu, L P Tsai, W C Wang, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui
|
May 1, 1996
Sex determination in infants with ambiguous genitalia using the polymerase chain reaction of an X-Y homologous region
C H Tsai, F J Tsai, W L Hwu, et al.
Human Mutation
|
August 31, 2002
A founder mutation (R254X) of SLC22A5 (OCTN2) in Chinese primary carnitine deficiency patients
Nelson L S Tang, W L Hwu, Rachel T Chan, et al.
Journal of Inherited Metabolic Disease
|
August 19, 2007
Deficiency of the carnitine transporter (OCTN2) with partial N-acetylglutamate synthase (NAGS) deficiency
W-L Hwu, Y-H Chien, N L S Tang, et al.
Page
of 8