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Pediatric Radiology
|
January 1, 1992
MRI of sequela of transverse myelitis
W C Shen, S K Lee, Y J Ho, et al.
Zhonghua Yi Xue Za Zhi = Chinese Medical Journal; Free China Ed
|
November 1, 1993
Juvenile and adult dermatomyositis among the Chinese: a comparative study
Y J Wang, Y P Lii, J L Lan, et al.
Neuropediatrics
|
October 9, 2002
A novel mutation in neonatal isolated sulphite oxidase deficiency
H F Lee, B S C Mak, C S Chi, et al.
Biochemical and Biophysical Research Communications
|
November 22, 1995
A novel mitochondrial DNA point mutation associated with mitochondrial encephalocardiomyopathy
F M Santorelli, S C Mak, M Vàzquez-Acevedo, et al.
American Journal of Human Genetics
|
May 1, 1996
Maternally inherited cardiomyopathy and hearing loss associated with a novel mutation in the mitochondrial tRNA(Lys) gene (G8363A)
F M Santorelli, S C Mak, M El-Schahawi, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui
|
November 1, 1994
Lesch-Nyhan Syndrome: report on two brothers
M T Yang, S C Mak, C S Chi, et al.
Annals of the New York Academy of Sciences
|
May 14, 2005
Vitellogenesis in the red crab, Charybdis feriatus: contributions from small vitellogenin transcripts (CfVg) and farnesoic acid stimulation of CfVg expression
Siu-Ming Chan, Abby S C Mak, Chi Lung Choi, et al.
Oncogene
|
February 15, 2011
P-cadherin cooperates with insulin-like growth factor-1 receptor to promote metastatic signaling of gonadotropin-releasing hormone in ovarian cancer via p120 catenin
L W T Cheung, A S C Mak, A N Y Cheung, et al.
Pediatric Research
|
May 1, 1996
Clinical heterogeneity associated with the mitochondrial DNA T8993C point mutation
F M Santorelli, S C Mak, M E Vazquez-Memije, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
October 26, 2012
Human female reproductive tract epithelial cell culture
Rachel W S Chan, Abby S C Mak, William S B Yeung, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 65) with videos related to
Sort By:
Page
of 7
Pediatric Radiology
|
January 1, 1992
MRI of sequela of transverse myelitis
W C Shen, S K Lee, Y J Ho, et al.
Zhonghua Yi Xue Za Zhi = Chinese Medical Journal; Free China Ed
|
November 1, 1993
Juvenile and adult dermatomyositis among the Chinese: a comparative study
Y J Wang, Y P Lii, J L Lan, et al.
Neuropediatrics
|
October 9, 2002
A novel mutation in neonatal isolated sulphite oxidase deficiency
H F Lee, B S C Mak, C S Chi, et al.
Biochemical and Biophysical Research Communications
|
November 22, 1995
A novel mitochondrial DNA point mutation associated with mitochondrial encephalocardiomyopathy
F M Santorelli, S C Mak, M Vàzquez-Acevedo, et al.
American Journal of Human Genetics
|
May 1, 1996
Maternally inherited cardiomyopathy and hearing loss associated with a novel mutation in the mitochondrial tRNA(Lys) gene (G8363A)
F M Santorelli, S C Mak, M El-Schahawi, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui
|
November 1, 1994
Lesch-Nyhan Syndrome: report on two brothers
M T Yang, S C Mak, C S Chi, et al.
Annals of the New York Academy of Sciences
|
May 14, 2005
Vitellogenesis in the red crab, Charybdis feriatus: contributions from small vitellogenin transcripts (CfVg) and farnesoic acid stimulation of CfVg expression
Siu-Ming Chan, Abby S C Mak, Chi Lung Choi, et al.
Oncogene
|
February 15, 2011
P-cadherin cooperates with insulin-like growth factor-1 receptor to promote metastatic signaling of gonadotropin-releasing hormone in ovarian cancer via p120 catenin
L W T Cheung, A S C Mak, A N Y Cheung, et al.
Pediatric Research
|
May 1, 1996
Clinical heterogeneity associated with the mitochondrial DNA T8993C point mutation
F M Santorelli, S C Mak, M E Vazquez-Memije, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
October 26, 2012
Human female reproductive tract epithelial cell culture
Rachel W S Chan, Abby S C Mak, William S B Yeung, et al.
Page
of 7