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M J Denton

Showing results (21-30 of 50) with videos related to

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Australian Paediatric Journal|December 1, 1988
Prenatal diagnosis and carrier detection by DNA studies in a Duchenne muscular dystrophy family with no living affected maleJ D Chen, M J Denton, S Serravalle, et al.
Australian and New Zealand Journal of Ophthalmology|May 1, 1990
Exclusion of the autosomal dominant retinitis pigmentosa gene from a substantial region of chromosome 1: study of a large Australian familyA Chand, J E Olsson, L Adams, et al.
Biomaterials|October 1, 1982
An experimental study of the use of a carbon fibre patch as a hernia prosthesis materialR J Minns, M J Denton, G H Dunstone, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1991
Description of X-linked megalocornea with identification of the gene locusD A Mackey, R G Buttery, G M Wise, et al.
The New Zealand Medical Journal|February 12, 1992
The prevalence of retinitis pigmentosa in Otago and SouthlandM L Bennett, G F Sanderson, R J Gardner, et al.
Journal of Medical Genetics|October 3, 1999
Autosomal recessive retinitis pigmentosa locus RP28 maps between D2S1337 and D2S286 on chromosome 2p11-p15 in an Indian familyS Gu, G Kumaramanickavel, C R Srikumari, et al.
Clinical Genetics|May 1, 1989
Non-allelic mutations in X-linked retinitis pigmentosaJ D Chen, P Dickinson, R Gray, et al.
Human Genetics|October 1, 1989
X-linked megalocornea: close linkage to DXS87 and DXS94J D Chen, D Mackey, H Fuller, et al.
Australian Paediatric Journal|January 1, 1988
Experience with DNA analysis in Duchenne and Becker muscular dystrophy families in NSWG Morgan, J A Donald, J Chen, et al.
The Australian and New Zealand Journal of Surgery|November 1, 1988
Extraperitoneal unilateral iliac artery bypass for chronic lower limb ischaemiaC Cham, K A Myers, D F Scott, et al.
Pageof 5

Showing results (21-30 of 50) with videos related to

Sort By:
Pageof 5
Australian Paediatric Journal|December 1, 1988
Prenatal diagnosis and carrier detection by DNA studies in a Duchenne muscular dystrophy family with no living affected maleJ D Chen, M J Denton, S Serravalle, et al.
Australian and New Zealand Journal of Ophthalmology|May 1, 1990
Exclusion of the autosomal dominant retinitis pigmentosa gene from a substantial region of chromosome 1: study of a large Australian familyA Chand, J E Olsson, L Adams, et al.
Biomaterials|October 1, 1982
An experimental study of the use of a carbon fibre patch as a hernia prosthesis materialR J Minns, M J Denton, G H Dunstone, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1991
Description of X-linked megalocornea with identification of the gene locusD A Mackey, R G Buttery, G M Wise, et al.
The New Zealand Medical Journal|February 12, 1992
The prevalence of retinitis pigmentosa in Otago and SouthlandM L Bennett, G F Sanderson, R J Gardner, et al.
Journal of Medical Genetics|October 3, 1999
Autosomal recessive retinitis pigmentosa locus RP28 maps between D2S1337 and D2S286 on chromosome 2p11-p15 in an Indian familyS Gu, G Kumaramanickavel, C R Srikumari, et al.
Clinical Genetics|May 1, 1989
Non-allelic mutations in X-linked retinitis pigmentosaJ D Chen, P Dickinson, R Gray, et al.
Human Genetics|October 1, 1989
X-linked megalocornea: close linkage to DXS87 and DXS94J D Chen, D Mackey, H Fuller, et al.
Australian Paediatric Journal|January 1, 1988
Experience with DNA analysis in Duchenne and Becker muscular dystrophy families in NSWG Morgan, J A Donald, J Chen, et al.
The Australian and New Zealand Journal of Surgery|November 1, 1988
Extraperitoneal unilateral iliac artery bypass for chronic lower limb ischaemiaC Cham, K A Myers, D F Scott, et al.
Pageof 5