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Molecular Vision
|
May 6, 1999
Identifying and mapping novel retinal-expressed ESTs from humans
K Malone, M M Sohocki, L S Sullivan, et al.
American Journal of Human Genetics
|
April 1, 1986
The anonymous polymorphic DNA clone D1S1, previously mapped to human chromosome 1p36 by in situ hybridization, is from chromosome 3 and is duplicated on chromosome 1
M E Goode, P vanTuinen, D H Ledbetter, et al.
American Journal of Human Genetics
|
August 1, 1992
Van der Woude syndrome and nonsyndromic cleft lip and palate
J T Hecht, Y Wang, S H Blanton, et al.
American Journal of Ophthalmology
|
November 13, 2001
Splice site mutation in the peripherin/RDS gene associated with pattern dystrophy of the retina
J E Sears, T A Aaberg, S P Daiger, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
June 23, 2001
Comparative analysis of aryl-hydrocarbon receptor interacting protein-like 1 (Aipl1), a gene associated with inherited retinal disease in humans
M M Sohocki, L S Sullivan, D L Tirpak, et al.
The American Journal of Cardiology
|
February 1, 1984
Increased frequency of coronary heart disease in relatives of wives of myocardial infarct survivors: assortative mating for lifestyle and risk factors?
L P ten Kate, H Boman, S P Daiger, et al.
Chinese Medical Journal
|
June 1, 1992
Linkage between Rh blood group and autosomal dominant retinitis pigmentosa in ten Chinese families
Y J Fei, S H Blanton, S P Daiger, et al.
American Journal of Human Genetics
|
July 1, 1981
Detection of genetic variation with radioactive ligands. IV. X-linked, polymorphic genetic variation of thyroxin-binding globulin (TBG)
S P Daiger, D P Rummel, L Wang, et al.
Progress in Clinical and Biological Research
|
January 1, 1987
DNA linkage studies of degenerative retinal diseases
S P Daiger, J R Heckenlively, R A Lewis, et al.
Ophthalmic Genetics
|
August 1, 2000
Visual phenotype in patients with Arg41Gln and ala196+1bp mutations in the CRX gene
R T Tzekov, M M Sohocki, S P Daiger, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 84) with videos related to
Sort By:
Page
of 9
Molecular Vision
|
May 6, 1999
Identifying and mapping novel retinal-expressed ESTs from humans
K Malone, M M Sohocki, L S Sullivan, et al.
American Journal of Human Genetics
|
April 1, 1986
The anonymous polymorphic DNA clone D1S1, previously mapped to human chromosome 1p36 by in situ hybridization, is from chromosome 3 and is duplicated on chromosome 1
M E Goode, P vanTuinen, D H Ledbetter, et al.
American Journal of Human Genetics
|
August 1, 1992
Van der Woude syndrome and nonsyndromic cleft lip and palate
J T Hecht, Y Wang, S H Blanton, et al.
American Journal of Ophthalmology
|
November 13, 2001
Splice site mutation in the peripherin/RDS gene associated with pattern dystrophy of the retina
J E Sears, T A Aaberg, S P Daiger, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
June 23, 2001
Comparative analysis of aryl-hydrocarbon receptor interacting protein-like 1 (Aipl1), a gene associated with inherited retinal disease in humans
M M Sohocki, L S Sullivan, D L Tirpak, et al.
The American Journal of Cardiology
|
February 1, 1984
Increased frequency of coronary heart disease in relatives of wives of myocardial infarct survivors: assortative mating for lifestyle and risk factors?
L P ten Kate, H Boman, S P Daiger, et al.
Chinese Medical Journal
|
June 1, 1992
Linkage between Rh blood group and autosomal dominant retinitis pigmentosa in ten Chinese families
Y J Fei, S H Blanton, S P Daiger, et al.
American Journal of Human Genetics
|
July 1, 1981
Detection of genetic variation with radioactive ligands. IV. X-linked, polymorphic genetic variation of thyroxin-binding globulin (TBG)
S P Daiger, D P Rummel, L Wang, et al.
Progress in Clinical and Biological Research
|
January 1, 1987
DNA linkage studies of degenerative retinal diseases
S P Daiger, J R Heckenlively, R A Lewis, et al.
Ophthalmic Genetics
|
August 1, 2000
Visual phenotype in patients with Arg41Gln and ala196+1bp mutations in the CRX gene
R T Tzekov, M M Sohocki, S P Daiger, et al.
Page
of 9