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W Y Hung

Showing results (31-40 of 116) with videos related to

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British Journal of Sports Medicine|July 28, 2005
Effects of weight bearing and non-weight bearing exercises on bone properties using calcaneal quantitative ultrasoundP S Yung, Y M Lai, P Y Tung, et al.
Neurology|January 30, 2009
Age and founder effect of SOD1 A4V mutation causing ALSM Saeed, Y Yang, H-X Deng, et al.
Australian Paediatric Journal|January 1, 1988
Update on the molecular genetics of Duchenne muscular dystrophyT Siddique, R Bartlett, M Pericak-Vance, et al.
Studies in Health Technology and Informatics|November 17, 2006
Lower degree of mineralization found in cortical bone of adolescent idiopathic scoliosis (AIS)H Y Yeung, L Qin, V W Y Hung, et al.
Archives of Osteoporosis|August 5, 2025
Longitudinal bone loss in the paretic leg and its contributing factors in individuals with chronic stroke: a 2-year prospective cohort studyHuixi Ouyang, Tiev Miller, Ling Qin, et al.
Human Molecular Genetics|August 1, 1994
Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneityA Hentati, M A Pericak-Vance, W Y Hung, et al.
Annals of Neurology|March 1, 1996
Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiencyA Hentati, H X Deng, W Y Hung, et al.
Nucleic Acids Research|July 25, 1988
RFLP for Duchenne muscular dystrophy cDNA clone 44-1N G Laing, T Siddique, R J Bartlett, et al.
Nucleic Acids Research|September 26, 1988
RFLP for Duchenne muscular dystrophy cDNA clone 30-2A P Walker, R J Bartlett, N G Laing, et al.
Human Molecular Genetics|June 1, 1995
Two novel SOD1 mutations in patients with familial amyotrophic lateral sclerosisH X Deng, J A Tainer, H Mitsumoto, et al.
Pageof 12

Showing results (31-40 of 116) with videos related to

Sort By:
Pageof 12
British Journal of Sports Medicine|July 28, 2005
Effects of weight bearing and non-weight bearing exercises on bone properties using calcaneal quantitative ultrasoundP S Yung, Y M Lai, P Y Tung, et al.
Neurology|January 30, 2009
Age and founder effect of SOD1 A4V mutation causing ALSM Saeed, Y Yang, H-X Deng, et al.
Australian Paediatric Journal|January 1, 1988
Update on the molecular genetics of Duchenne muscular dystrophyT Siddique, R Bartlett, M Pericak-Vance, et al.
Studies in Health Technology and Informatics|November 17, 2006
Lower degree of mineralization found in cortical bone of adolescent idiopathic scoliosis (AIS)H Y Yeung, L Qin, V W Y Hung, et al.
Archives of Osteoporosis|August 5, 2025
Longitudinal bone loss in the paretic leg and its contributing factors in individuals with chronic stroke: a 2-year prospective cohort studyHuixi Ouyang, Tiev Miller, Ling Qin, et al.
Human Molecular Genetics|August 1, 1994
Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneityA Hentati, M A Pericak-Vance, W Y Hung, et al.
Annals of Neurology|March 1, 1996
Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiencyA Hentati, H X Deng, W Y Hung, et al.
Nucleic Acids Research|July 25, 1988
RFLP for Duchenne muscular dystrophy cDNA clone 44-1N G Laing, T Siddique, R J Bartlett, et al.
Nucleic Acids Research|September 26, 1988
RFLP for Duchenne muscular dystrophy cDNA clone 30-2A P Walker, R J Bartlett, N G Laing, et al.
Human Molecular Genetics|June 1, 1995
Two novel SOD1 mutations in patients with familial amyotrophic lateral sclerosisH X Deng, J A Tainer, H Mitsumoto, et al.
Pageof 12