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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 male
J 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 family
A 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 material
R 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 locus
D 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 Southland
M 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 family
S Gu, G Kumaramanickavel, C R Srikumari, et al.
Clinical Genetics
|
May 1, 1989
Non-allelic mutations in X-linked retinitis pigmentosa
J D Chen, P Dickinson, R Gray, et al.
Human Genetics
|
October 1, 1989
X-linked megalocornea: close linkage to DXS87 and DXS94
J 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 NSW
G 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 ischaemia
C Cham, K A Myers, D F Scott, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 50) with videos related to
Sort By:
Page
of 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 male
J 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 family
A 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 material
R 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 locus
D 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 Southland
M 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 family
S Gu, G Kumaramanickavel, C R Srikumari, et al.
Clinical Genetics
|
May 1, 1989
Non-allelic mutations in X-linked retinitis pigmentosa
J D Chen, P Dickinson, R Gray, et al.
Human Genetics
|
October 1, 1989
X-linked megalocornea: close linkage to DXS87 and DXS94
J 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 NSW
G 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 ischaemia
C Cham, K A Myers, D F Scott, et al.
Page
of 5