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American Journal of Human Genetics
|
May 1, 1988
The use of field-inversion gel electrophoresis for deletion detection in Duchenne muscular dystrophy
J D Chen, M J Denton, G Morgan, et al.
Human Molecular Genetics
|
June 1, 1993
Autosomal dominant 'sector' retinitis pigmentosa due to a point mutation predicting an Asn-15-Ser substitution of rhodopsin
H Kranich, S Bartkowski, M J Denton, et al.
Lancet (London, England)
|
January 3, 1987
Recombination between Duchenne muscular dystrophy and DNA marker DXS164 (pERT87)
J A Donald, G Morgan, J D Chen, et al.
Human Genetics
|
January 1, 1988
Analysis of linkage relationships of X-linked retinitis pigmentosa with the following Xp loci: L1.28, OTC, 754, XJ-1.1, pERT87, and C7
M J Denton, J D Chen, S Serravalle, et al.
Human Molecular Genetics
|
July 1, 1994
Three novel rhodopsin mutations (C110F, L131P, A164V) in patients with autosomal dominant retinitis pigmentosa
S Fuchs, H Kranich, M J Denton, et al.
Annals of Vascular Surgery
|
May 1, 1993
Multivariate Cox regression analysis of covariates for patency rates after femorodistal vein bypass grafting
K A Myers, J A Fuller, D F Scott, et al.
European Journal of Vascular Surgery
|
August 1, 1987
Palpation of the femoral and popliteal pulses: a study of the accuracy as assessed by agreement between multiple observers
K A Myers, D F Scott, T J Devine, et al.
Nature Genetics
|
September 1, 1994
Missense rhodopsin mutation in a family with recessive RP
G Kumaramanickavel, M Maw, M J Denton, et al.
Journal of Medical Genetics
|
May 1, 1995
Oguchi disease: suggestion of linkage to markers on chromosome 2q
M A Maw, S John, S Jablonka, et al.
Cardiovascular Surgery (London, England)
|
August 1, 1996
Clinical and vascular laboratory determinants for outcome after infrainguinal atherectomy
K A Myers, G H Zeng, R W Ziegenbein, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 50) with videos related to
Sort By:
Page
of 5
American Journal of Human Genetics
|
May 1, 1988
The use of field-inversion gel electrophoresis for deletion detection in Duchenne muscular dystrophy
J D Chen, M J Denton, G Morgan, et al.
Human Molecular Genetics
|
June 1, 1993
Autosomal dominant 'sector' retinitis pigmentosa due to a point mutation predicting an Asn-15-Ser substitution of rhodopsin
H Kranich, S Bartkowski, M J Denton, et al.
Lancet (London, England)
|
January 3, 1987
Recombination between Duchenne muscular dystrophy and DNA marker DXS164 (pERT87)
J A Donald, G Morgan, J D Chen, et al.
Human Genetics
|
January 1, 1988
Analysis of linkage relationships of X-linked retinitis pigmentosa with the following Xp loci: L1.28, OTC, 754, XJ-1.1, pERT87, and C7
M J Denton, J D Chen, S Serravalle, et al.
Human Molecular Genetics
|
July 1, 1994
Three novel rhodopsin mutations (C110F, L131P, A164V) in patients with autosomal dominant retinitis pigmentosa
S Fuchs, H Kranich, M J Denton, et al.
Annals of Vascular Surgery
|
May 1, 1993
Multivariate Cox regression analysis of covariates for patency rates after femorodistal vein bypass grafting
K A Myers, J A Fuller, D F Scott, et al.
European Journal of Vascular Surgery
|
August 1, 1987
Palpation of the femoral and popliteal pulses: a study of the accuracy as assessed by agreement between multiple observers
K A Myers, D F Scott, T J Devine, et al.
Nature Genetics
|
September 1, 1994
Missense rhodopsin mutation in a family with recessive RP
G Kumaramanickavel, M Maw, M J Denton, et al.
Journal of Medical Genetics
|
May 1, 1995
Oguchi disease: suggestion of linkage to markers on chromosome 2q
M A Maw, S John, S Jablonka, et al.
Cardiovascular Surgery (London, England)
|
August 1, 1996
Clinical and vascular laboratory determinants for outcome after infrainguinal atherectomy
K A Myers, G H Zeng, R W Ziegenbein, et al.
Page
of 5