-
1
-
-
0021702822
-
Vision in the elderly and its use in the social environment
-
Hakkinen, L. (1984) Vision in the elderly and its use in the social environment. Scand. J. Soc. Med., 35 (Suppl), 5-60.
-
(1984)
Scand. J. Soc. Med.
, vol.35
, Issue.SUPPL.
, pp. 5-60
-
-
Hakkinen, L.1
-
2
-
-
0017704582
-
The Framingham eye study. I. Outline and major prevalence findings
-
Kahn, H.A., Leibowitz, H.M., Ganley, J.P., Kini, M.M., Colton, T., Nickerson, R.S. and Dawber, T.R. (1977) The Framingham Eye Study. I. Outline and major prevalence findings. Am. J. Epidemiol., 106, 17-32.
-
(1977)
Am. J. Epidemiol.
, vol.106
, pp. 17-32
-
-
Kahn, H.A.1
Leibowitz, H.M.2
Ganley, J.P.3
Kini, M.M.4
Colton, T.5
Nickerson, R.S.6
Dawber, T.R.7
-
3
-
-
0020067097
-
Cataracts and macular degeneration in older Americans
-
Klein, B. and Klein, R. (1982) Cataracts and macular degeneration in older Americans. Arch. Ophthalmol., 100, 571-573.
-
(1982)
Arch. Ophthalmol.
, vol.100
, pp. 571-573
-
-
Klein, B.1
Klein, R.2
-
4
-
-
0019949978
-
Prevalence of ocular disease in a population study of subjects 65 years old and older
-
Martinez, G. and Campbell, A. (1982) Prevalence of ocular disease in a population study of subjects 65 years old and older. Am. J. Ophthalmol., 94, 181-189.
-
(1982)
Am. J. Ophthalmol.
, vol.94
, pp. 181-189
-
-
Martinez, G.1
Campbell, A.2
-
5
-
-
0018966646
-
Senile lens and senile macular changes in a population-based sample
-
Sperduto, R. and Seigel, D. (1980) Senile lens and senile macular changes in a population-based sample. Am. J. Ophthalmol., 90, 86-91.
-
(1980)
Am. J. Ophthalmol.
, vol.90
, pp. 86-91
-
-
Sperduto, R.1
Seigel, D.2
-
6
-
-
0024801823
-
Age-related macular degeneration. Macular changes, prevalence and sex ratio. An epidemiological study of 1000 aged individuals
-
Vinding, T. (1989) Age-related macular degeneration. Macular changes, prevalence and sex ratio. An epidemiological study of 1000 aged individuals. Acta Ophthalmol., 67, 609-616.
-
(1989)
Acta Ophthalmol.
, vol.67
, pp. 609-616
-
-
Vinding, T.1
-
7
-
-
0032518733
-
Relation of smoking to the incidence of age-related maculopathy. The Beaver Dam eye study
-
Klein, R., Klein, B.E. and Moss, S.E. (1998) Relation of smoking to the incidence of age-related maculopathy. The Beaver Dam Eye Study. Am. J. Epidemiol., 147, 103-110.
-
(1998)
Am. J. Epidemiol.
, vol.147
, pp. 103-110
-
-
Klein, R.1
Klein, B.E.2
Moss, S.E.3
-
8
-
-
0017643879
-
Changes in the choriocapillaris associated with senile macular degeneration
-
Kornzweig, A. (1977) Changes in the choriocapillaris associated with senile macular degeneration. Ann. Ophthalmol., 9, 753-756.
-
(1977)
Ann. Ophthalmol.
, vol.9
, pp. 753-756
-
-
Kornzweig, A.1
-
9
-
-
0023919632
-
Age-related macular degeneration
-
Bressler, N., Bressler, S. and Fine, S. (1988) Age-related macular degeneration. Surv. Ophthalmol., 32, 375-413.
-
(1988)
Surv. Ophthalmol.
, vol.32
, pp. 375-413
-
-
Bressler, N.1
Bressler, S.2
Fine, S.3
-
10
-
-
0017078404
-
Aging and degeneration in the macular region: A clinicopathological study
-
Sarks, S. (1976) Aging and degeneration in the macular region: a clinicopathological study. Br. J. Ophthalmol., 60, 324-341.
-
(1976)
Br. J. Ophthalmol.
, vol.60
, pp. 324-341
-
-
Sarks, S.1
-
11
-
-
0019253913
-
Softening of drusen and subretinal neovascularization
-
Sarks, S., Van Driel, D., Maxwell, L. and Killingsworth, M. (1980) Softening of drusen and subretinal neovascularization. Trans. Ophthalmol. Soc. UK. 100, 414-422.
-
(1980)
Trans. Ophthalmol. Soc. UK
, vol.100
, pp. 414-422
-
-
Sarks, S.1
Van Driel, D.2
Maxwell, L.3
Killingsworth, M.4
-
12
-
-
0019018431
-
Drusen and their relationship to senile macular degeneration
-
Sarks, S.H. (1980) Drusen and their relationship to senile macular degeneration. Aust. J. Ophthalmol., 8, 117-130.
-
(1980)
Aust. J. Ophthalmol.
, vol.8
, pp. 117-130
-
-
Sarks, S.H.1
-
13
-
-
0020071301
-
Drusen in patients predisposing to geographic atrophy of the retinal pigment epithelium
-
Sarks, S. (1982) Drusen in patients predisposing to geographic atrophy of the retinal pigment epithelium. Aust. J. Ophthalmol., 10, 91-97.
-
(1982)
Aust. J. Ophthalmol.
, vol.10
, pp. 91-97
-
-
Sarks, S.1
-
14
-
-
0024151007
-
Evolution of geographic atrophy of the retinal pigment epithelium
-
Sarks, J., Sarks, S. and Killingsworth, M. (1988) Evolution of geographic atrophy of the retinal pigment epithelium. Eye, 2, 552-577.
-
(1988)
Eye
, vol.2
, pp. 552-577
-
-
Sarks, J.1
Sarks, S.2
Killingsworth, M.3
-
15
-
-
0021071902
-
The recurrence of neovascularization and late visual failure in senile disciform lesions
-
Chisholm, I. (1983) The recurrence of neovascularization and late visual failure in senile disciform lesions. Trans. Ophthalmol. Soc. UK. 103, 354-359.
-
(1983)
Trans. Ophthalmol. Soc. UK
, vol.103
, pp. 354-359
-
-
Chisholm, I.1
-
16
-
-
0342720825
-
The genetics of age-relaled maculopathy
-
Hollyfield, J., Anderson, R. and LaVail, M. (eds), Plenum Press, New York, NY
-
Gorin, M., Sarneso, C., Paul, T., Ngo, J. and Weeks, D. (1993) The genetics of age-relaled maculopathy. In Hollyfield, J., Anderson, R. and LaVail, M. (eds), Retinal Degeneration. Plenum Press, New York, NY, pp. 35-47.
-
(1993)
Retinal Degeneration
, pp. 35-47
-
-
Gorin, M.1
Sarneso, C.2
Paul, T.3
Ngo, J.4
Weeks, D.5
-
17
-
-
0031022320
-
Familial aggregation of age-related maculopathy
-
Seddon, J.M., Ajani, U.A. and Mitchell, B.D. (1997) Familial aggregation of age-related maculopathy. Am. J. Ophthalmol., 123, 199-206.
-
(1997)
Am. J. Ophthalmol.
, vol.123
, pp. 199-206
-
-
Seddon, J.M.1
Ajani, U.A.2
Mitchell, B.D.3
-
19
-
-
0032773711
-
Age related macular degeneration in monozygotic twins and their spouses in Iceland
-
Gottfredsdottir, M.S., Sverrisson, T., Musch, D.C. and Stefansson, E. (1999) Age related macular degeneration in monozygotic twins and their spouses in Iceland. Acta Ophthalmol. Scand., 77, 422-425.
-
(1999)
Acta Ophthalmol. Scand.
, vol.77
, pp. 422-425
-
-
Gottfredsdottir, M.S.1
Sverrisson, T.2
Musch, D.C.3
Stefansson, E.4
-
20
-
-
0028875171
-
A twin study of age-related macular degeneration
-
Meyers, S.M., Greene, T. and Gutman, F.A. (1995) A twin study of age-related macular degeneration. Am. J. Ophthalmol., 120, 757-766.
-
(1995)
Am. J. Ophthalmol.
, vol.120
, pp. 757-766
-
-
Meyers, S.M.1
Greene, T.2
Gutman, F.A.3
-
21
-
-
26144435336
-
Age-related macular degeneration in monozygotic twins and their spouses
-
Sverrisson, T., Gottfredsdottir, M.S. and Stefansson, E. (1995) Age-related macular degeneration in monozygotic twins and their spouses. Invest. Ophthalmol. Vis. Sci., 36, S10.
-
(1995)
Invest. Ophthalmol. Vis. Sci.
, vol.36
-
-
Sverrisson, T.1
Gottfredsdottir, M.S.2
Stefansson, E.3
-
22
-
-
0028244159
-
Heredity and age-related macular degeneration. Observations in monozygotic twins
-
Klein, M.L., Mauldin, W.M. and Stoumbos, V.D. (1994) Heredity and age-related macular degeneration. Observations in monozygotic twins. Arch. Ophthalmol., 112, 932-937.
-
(1994)
Arch. Ophthalmol.
, vol.112
, pp. 932-937
-
-
Klein, M.L.1
Mauldin, W.M.2
Stoumbos, V.D.3
-
23
-
-
0028298094
-
Sibling correlations and segregation analysis of age-related maculopathy: The Beaver Dam Eye Study
-
Heiba, I.M., Elston, R.C., Klein, B.E. and Klein, R. (1994) Sibling correlations and segregation analysis of age-related maculopathy: the Beaver Dam Eye Study. Genet. Epidemiol., 11, 51-67.
-
(1994)
Genet. Epidemiol.
, vol.11
, pp. 51-67
-
-
Heiba, I.M.1
Elston, R.C.2
Klein, B.E.3
Klein, R.4
-
24
-
-
0015816276
-
Drusen and disciform macular detachment and degeneration
-
Gass, J.D.M. (1973) Drusen and disciform macular detachment and degeneration. Arch. Ophthalmol., 90, 206-217.
-
(1973)
Arch. Ophthalmol.
, vol.90
, pp. 206-217
-
-
Gass, J.D.M.1
-
25
-
-
0028804575
-
A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degeneration
-
Gorin, M.B., Jackson, K.E., Ferrell, R.E., Sheffield, V.C., Jacobson, S.G., Gass, J.D., Mitchell, E. and Stone, E.M. (1995) A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degeneration. Ophthalmology, 102, 246-255.
-
(1995)
Ophthalmology
, vol.102
, pp. 246-255
-
-
Gorin, M.B.1
Jackson, K.E.2
Ferrell, R.E.3
Sheffield, V.C.4
Jacobson, S.G.5
Gass, J.D.6
Mitchell, E.7
Stone, E.M.8
-
26
-
-
0028069944
-
RDS gene mutations causing retinitis pigmentosa or macular degeneration lead to the same abnormality in photoreceptor function
-
Kemp, C.M., Jacobson, S.G., Cideciyan, A.V., Kimura, A.E., Sheffield, V.C. and Stone, E.M. (1994) RDS gene mutations causing retinitis pigmentosa or macular degeneration lead to the same abnormality in photoreceptor function. Invest. Ophthalmol. Vis. Sci., 35, 3154-3162.
-
(1994)
Invest. Ophthalmol. Vis. Sci.
, vol.35
, pp. 3154-3162
-
-
Kemp, C.M.1
Jacobson, S.G.2
Cideciyan, A.V.3
Kimura, A.E.4
Sheffield, V.C.5
Stone, E.M.6
-
27
-
-
0027447531
-
Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy
-
Wells, J., Wroblewski, J., Keen, J., Inglehearn, C., Jubb, C., Eckstein, A., Jay, M., Arden, G., Bhattacharya, S., Fitzke, F. et al. (1993) Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy. Nature Genet., 3, 213-218.
-
(1993)
Nature Genet.
, vol.3
, pp. 213-218
-
-
Wells, J.1
Wroblewski, J.2
Keen, J.3
Inglehearn, C.4
Jubb, C.5
Eckstein, A.6
Jay, M.7
Arden, G.8
Bhattacharya, S.9
Fitzke, F.10
-
28
-
-
0028010027
-
Macular dystrophy associated with mutations at codon 172 in the human retinal degeneration slow gene
-
Wroblewski, J.J., Wells, J.A.R., Eckstein, A., Fitzke, F., Jubb, C., Keen, T.J., Inglehearn, C., Bhattacharya, S., Arden, G.B., Jay, M. et al. (1994) Macular dystrophy associated with mutations at codon 172 in the human retinal degeneration slow gene. Ophthalmology, 101, 12-22.
-
(1994)
Ophthalmology
, vol.101
, pp. 12-22
-
-
Wroblewski, J.J.1
Wells, J.A.R.2
Eckstein, A.3
Fitzke, F.4
Jubb, C.5
Keen, T.J.6
Inglehearn, C.7
Bhattacharya, S.8
Arden, G.B.9
Jay, M.10
-
29
-
-
0028097367
-
Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophy
-
Weber, B.H., Vogt, G., Pruett, R.C., Stohr, H. and Felbor, U. (1994) Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophy. Nature Genet., 8, 352-356.
-
(1994)
Nature Genet.
, vol.8
, pp. 352-356
-
-
Weber, B.H.1
Vogt, G.2
Pruett, R.C.3
Stohr, H.4
Felbor, U.5
-
30
-
-
4244213475
-
Mutational analysis of TIMP3 in Sorsby's fundus dystrophy (SFD) and age-related macular dystrophy (AMD)
-
Weber, B.H.F., Felbor, U., Schneider, U. and Doepner, D. (1995) Mutational analysis of TIMP3 in Sorsby's fundus dystrophy (SFD) and age-related macular dystrophy (AMD). Invest. Ophthalmol. Vis. Sci., 36, S1064.
-
(1995)
Invest. Ophthalmol. Vis. Sci.
, vol.36
-
-
Weber, B.H.F.1
Felbor, U.2
Schneider, U.3
Doepner, D.4
-
31
-
-
0030962268
-
Exclusion of TIMP3 as a candidate locus in age-related macular degeneration
-
De La Paz, M.A., Pericak-Vance, M.A., Lennon, F., Haines, J.L. and Seddon, J.M. (1997) Exclusion of TIMP3 as a candidate locus in age-related macular degeneration. Invest. Ophthalmol. Vis. Sci., 38, 1060-1065.
-
(1997)
Invest. Ophthalmol. Vis. Sci.
, vol.38
, pp. 1060-1065
-
-
De La Paz, M.A.1
Pericak-Vance, M.A.2
Lennon, F.3
Haines, J.L.4
Seddon, J.M.5
-
32
-
-
0030949922
-
Evaluation of the gene encoding the tissue inhibitor of metalloproteinases-3 in various maculopathies
-
Felbor, U., Doepner, D., Schneider, U., Zrenner, E. and Weber, B.H. (1997) Evaluation of the gene encoding the tissue inhibitor of metalloproteinases-3 in various maculopathies. Invest. Ophthalmol. Vis. Sci., 38, 1054-1059.
-
(1997)
Invest. Ophthalmol. Vis. Sci.
, vol.38
, pp. 1054-1059
-
-
Felbor, U.1
Doepner, D.2
Schneider, U.3
Zrenner, E.4
Weber, B.H.5
-
33
-
-
0012119330
-
Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration
-
Allikmets, R., Shroyer, N., Singh, N., Seddon, J., Lewis, R., Bernstein, P., Peiffer, A., Zabriskie, N., Li, Y., Hutchinson, A., Dean, M., Lupski, J. and Leppert, M. (1997) Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration. Science, 277, 1805-1807.
-
(1997)
Science
, vol.277
, pp. 1805-1807
-
-
Allikmets, R.1
Shroyer, N.2
Singh, N.3
Seddon, J.4
Lewis, R.5
Bernstein, P.6
Peiffer, A.7
Zabriskie, N.8
Li, Y.9
Hutchinson, A.10
Dean, M.11
Lupski, J.12
Leppert, M.13
-
34
-
-
12944255842
-
Analysis of the Stargardt disease gene (ABCR) in age-related macular degeneration
-
De La Paz, M.A., Guy, V.K., Abou-Donia, S., Heinis, R., Bracken, B., Vance, J.M., Gilbert, J.R., Gass, J.D., Haines, J.L. and Pericak-Vance, M.A. (1999) Analysis of the Stargardt disease gene (ABCR) in age-related macular degeneration. Ophthalmology, 106, 1531-1536.
-
(1999)
Ophthalmology
, vol.106
, pp. 1531-1536
-
-
De La Paz, M.A.1
Guy, V.K.2
Abou-Donia, S.3
Heinis, R.4
Bracken, B.5
Vance, J.M.6
Gilbert, J.R.7
Gass, J.D.8
Haines, J.L.9
Pericak-Vance, M.A.10
-
35
-
-
0032796491
-
Age-related macular degeneration in grandparents of patients with Stargardt disease: Genetic study
-
Souied, E.H., Ducroq, D., Gerber, S., Ghazi, I., Rozet, J.M., Perrault, I., Munnich, A., Dufier, J.L., Coscas, G., Soubrane, G. and Kaplan, J. (1999) Age-related macular degeneration in grandparents of patients with Stargardt disease: genetic study. Am. J. Ophthalmol., 128, 173-178.
-
(1999)
Am. J. Ophthalmol.
, vol.128
, pp. 173-178
-
-
Souied, E.H.1
Ducroq, D.2
Gerber, S.3
Ghazi, I.4
Rozet, J.M.5
Perrault, I.6
Munnich, A.7
Dufier, J.L.8
Coscas, G.9
Soubrane, G.10
Kaplan, J.11
-
36
-
-
0031795853
-
Allelic variation in ABCR associated with Stargardt disease but not age-related macular degeneration
-
Stone, E., Webster, A., Vandenburgh, K., Streb, L., Hockey, R., Lotery, A. and Sheffield, V. (1988) Allelic variation in ABCR associated with Stargardt disease but not age-related macular degeneration. Nature Genet., 20, 328-329.
-
(1988)
Nature Genet.
, vol.20
, pp. 328-329
-
-
Stone, E.1
Webster, A.2
Vandenburgh, K.3
Streb, L.4
Hockey, R.5
Lotery, A.6
Sheffield, V.7
-
37
-
-
0032231956
-
Genetic association of apolipoprotein E with age-related macular degeneration
-
Klaver, C.C., Kliffen, M., van Duijn, C., Hofman, A., Cruts, M., Grobbee, D.E., van Broeckhoven, C. and de Jong, P.T. (1998) Genetic association of apolipoprotein E with age-related macular degeneration. Am. J. Hum. Genet., 63, 200-206.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 200-206
-
-
Klaver, C.C.1
Kliffen, M.2
Van Duijn, C.3
Hofman, A.4
Cruts, M.5
Grobbee, D.E.6
Van Broeckhoven, C.7
De Jong, P.T.8
-
38
-
-
0032014838
-
The epsilon4 allele of the apolipoprotein E gene as a potential protective factor for exudative age-related macular degeneration
-
Souied, E.H., Benlian, P., Amouyel, P., Feingold, J., Lagarde, J.P., Munnich, A., Kaplan, J., Coscas, G. and Soubrane, G. (1998) The epsilon4 allele of the apolipoprotein E gene as a potential protective factor for exudative age-related macular degeneration. Am. J. Ophthalmol., 125, 353-359.
-
(1998)
Am. J. Ophthalmol.
, vol.125
, pp. 353-359
-
-
Souied, E.H.1
Benlian, P.2
Amouyel, P.3
Feingold, J.4
Lagarde, J.P.5
Munnich, A.6
Kaplan, J.7
Coscas, G.8
Soubrane, G.9
-
39
-
-
0032468842
-
Age-related macular degeneration. Clinical features in a large family and linkage to chromosome 1q.
-
Klein, M.L., Schultz, D.W., Edwards, A., Matise, T.C., Rust, K., Berselli, C.B., Trzupek, K., Weleber, R.G., Ott, J., Wirtz, M.K. and Acott, T.S. (1998) Age-related macular degeneration. Clinical features in a large family and linkage to chromosome 1q.Arch. Ophthalmol., 116, 1082-1088.
-
(1998)
Arch. Ophthalmol.
, vol.116
, pp. 1082-1088
-
-
Klein, M.L.1
Schultz, D.W.2
Edwards, A.3
Matise, T.C.4
Rust, K.5
Berselli, C.B.6
Trzupek, K.7
Weleber, R.G.8
Ott, J.9
Wirtz, M.K.10
Acott, T.S.11
-
40
-
-
0033833739
-
A new locus for drusen with macular degeneration maps to chromosome 6
-
in press
-
Kniazeva, M., Traboulsi, E.I., Stefko, S.T., Gorin, M.B., Blaschak, C.J., Cutting, G., Han, M. and Zhang, K. (2000) A new locus for drusen with macular degeneration maps to chromosome 6. Am. J. Ophthalmol, in press.
-
(2000)
Am. J. Ophthalmol
-
-
Kniazeva, M.1
Traboulsi, E.I.2
Stefko, S.T.3
Gorin, M.B.4
Blaschak, C.J.5
Cutting, G.6
Han, M.7
Zhang, K.8
-
41
-
-
0020508565
-
Senile macular degeneration: A case-control study
-
Hyman, L.G., Lilienfeld, A.M., Ferris, F.L.I. and Fine, S.L. (1983) Senile macular degeneration: a case-control study. Am. J. Epidemiol., 118, 213-227.
-
(1983)
Am. J. Epidemiol.
, vol.118
, pp. 213-227
-
-
Hyman, L.G.1
Lilienfeld, A.M.2
Ferris, F.L.I.3
Fine, S.L.4
-
42
-
-
0019215047
-
The Framingham Eye Study monograph: An ophthalmological and epidemiological study of cataract, glaucoma, diabetic retinopathy, macular degeneration and visual acuity in a general population of 2631 adults, 1973-1975
-
Leibowitz, H.M., Krueger, D.E., Maunder, L.R., Milton, R.C., Kini, M.M., Kahn, H.A., Nickerson, R.J., Pool, J., Colton, T.L., Ganley, J.P. et al. (1980) The Framingham Eye Study monograph: an ophthalmological and epidemiological study of cataract, glaucoma, diabetic retinopathy, macular degeneration and visual acuity in a general population of 2631 adults, 1973-1975. Surv. Ophthalmol., 24, 335-610.
-
(1980)
Surv. Ophthalmol.
, vol.24
, pp. 335-610
-
-
Leibowitz, H.M.1
Krueger, D.E.2
Maunder, L.R.3
Milton, R.C.4
Kini, M.M.5
Kahn, H.A.6
Nickerson, R.J.7
Pool, J.8
Colton, T.L.9
Ganley, J.P.10
-
43
-
-
0023200919
-
Study of aging macular degeneration in China
-
Wu, L. (1987) Study of aging macular degeneration in China. Jpn. J. Ophthalmol., 31, 349-367.
-
(1987)
Jpn. J. Ophthalmol.
, vol.31
, pp. 349-367
-
-
Wu, L.1
-
44
-
-
0025219503
-
Visual impairment of age-related macular degeneration. An epidemiological study of 1000 aged individuals
-
Vinding, T. (1990) Visual impairment of age-related macular degeneration. An epidemiological study of 1000 aged individuals. Acta Ophthalmol., 68, 162-167.
-
(1990)
Acta Ophthalmol.
, vol.68
, pp. 162-167
-
-
Vinding, T.1
-
45
-
-
0031798611
-
A practice-based survey of familial age-related maculopathy
-
Keverline, M.R., Mah, T.S., Keverline, P.O. and Gorin, M.B. (1998) A practice-based survey of familial age-related maculopathy. Ophthalmic Genet., 19, 19-26.
-
(1998)
Ophthalmic Genet.
, vol.19
, pp. 19-26
-
-
Keverline, M.R.1
Mah, T.S.2
Keverline, P.O.3
Gorin, M.B.4
-
46
-
-
14444283397
-
Identification of a gene that causes primary open angle glaucoma
-
Stone, E.M., Fingert, J.H., Alward, W.L.M., Nguyen, T.D., Polansky, J.R., Sunden, S.L.F., Nishimura, D., Clark, A.F., Nystuen, A., Nichols, B.E. et al. (1997) Identification of a gene that causes primary open angle glaucoma. Science, 275, 668-670.
-
(1997)
Science
, vol.275
, pp. 668-670
-
-
Stone, E.M.1
Fingert, J.H.2
Alward, W.L.M.3
Nguyen, T.D.4
Polansky, J.R.5
Sunden, S.L.F.6
Nishimura, D.7
Clark, A.F.8
Nystuen, A.9
Nichols, B.E.10
-
47
-
-
0026676630
-
Region and age-dependent variation in susceptibility of the human retina to lipid peroxidation
-
De La Paz, M. and Anderson, R.E. (1992) Region and age-dependent variation in susceptibility of the human retina to lipid peroxidation. Invest. Ophthalmol. Vis. Sci., 33, 3497-3499.
-
(1992)
Invest. Ophthalmol. Vis. Sci.
, vol.33
, pp. 3497-3499
-
-
De La Paz, M.1
Anderson, R.E.2
-
48
-
-
0028141466
-
The human plasma glutathione peroxidase-encoding gene: Organization, sequence and localization to chromosome 5q32
-
Yoshimura, S., Suemizu, H., Taniguchi, Y., Arimori, K., Kawabe, N. and Moriuchi, T. (1994) The human plasma glutathione peroxidase-encoding gene: organization, sequence and localization to chromosome 5q32. Gene, 145, 293-297.
-
(1994)
Gene
, vol.145
, pp. 293-297
-
-
Yoshimura, S.1
Suemizu, H.2
Taniguchi, Y.3
Arimori, K.4
Kawabe, N.5
Moriuchi, T.6
-
49
-
-
0025156824
-
Immunohistochemical localization of peroxidative enzymes in ocular tissue
-
Atalla, L.R., Sevanian, A. and Rao, N.A. (1990) Immunohistochemical localization of peroxidative enzymes in ocular tissue. CLAO J., 16, S30-S33.
-
(1990)
CLAO J.
, vol.16
-
-
Atalla, L.R.1
Sevanian, A.2
Rao, N.A.3
-
50
-
-
0026695198
-
Lipid peroxidation and antioxidant enzymatic systems in rat retina as a function of age
-
Castorina, C., Campisi, A., Di Giacomo, C., Sorrenti, V., Russo, A. and Vanella, A. (1992) Lipid peroxidation and antioxidant enzymatic systems in rat retina as a function of age. Neurochem. Res., 17, 599-604.
-
(1992)
Neurochem. Res.
, vol.17
, pp. 599-604
-
-
Castorina, C.1
Campisi, A.2
Di Giacomo, C.3
Sorrenti, V.4
Russo, A.5
Vanella, A.6
-
51
-
-
0032521155
-
Glutathione in human plasma: Decline in association with aging, age-related macular degeneration and diabetes
-
Samiec, P.S., Drews-Botsch, C., Flagg, E.W., Kurtz, J.C., Sternberg Jr, P., Reed, R.L. and Jones, D.P. (1998) Glutathione in human plasma: decline in association with aging, age-related macular degeneration and diabetes. Free Radic. Biol. Med., 24, 699-704.
-
(1998)
Free Radic. Biol. Med.
, vol.24
, pp. 699-704
-
-
Samiec, P.S.1
Drews-Botsch, C.2
Flagg, E.W.3
Kurtz, J.C.4
Sternberg P., Jr.5
Reed, R.L.6
Jones, D.P.7
-
52
-
-
4244121442
-
Glutathione peroxidase 3: Identification of promoter region polymorphisms and association with age-related maculopathy
-
Conley, Y.P., Gorin, M.B., Mah, T.S., Weeks, D.E. and Ferrell, R.E. (1999) Glutathione peroxidase 3: identification of promoter region polymorphisms and association with age-related maculopathy. Am. J. Hum. Genet., 65, A104.
-
(1999)
Am. J. Hum. Genet.
, vol.65
-
-
Conley, Y.P.1
Gorin, M.B.2
Mah, T.S.3
Weeks, D.E.4
Ferrell, R.E.5
-
53
-
-
0033941023
-
A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data
-
Douglas, J.A., Boehnke, M. and Lange, K. (2000) A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data. Am. J. Hum. Genet., 66, 1287-1297.
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 1287-1297
-
-
Douglas, J.A.1
Boehnke, M.2
Lange, K.3
-
54
-
-
0028934221
-
An international classification and grading system for age-related maculopathy and age-related macular degeneration
-
The International ARM Epidemiological Study Group
-
Bird, A.C., Bressler, N.M., Bressler, S.B., Chisholm, I.H., Coscas, G., Davis, M.D., de Jong, P.T., Klaver, C.C., Klein, B.E., Klein, R. et al. (1995) An international classification and grading system for age-related maculopathy and age-related macular degeneration. The International ARM Epidemiological Study Group. Surv. Ophthalmol., 39, 367-374.
-
(1995)
Surv. Ophthalmol.
, vol.39
, pp. 367-374
-
-
Bird, A.C.1
Bressler, N.M.2
Bressler, S.B.3
Chisholm, I.H.4
Coscas, G.5
Davis, M.D.6
De Jong, P.T.7
Klaver, C.C.8
Klein, B.E.9
Klein, R.10
-
55
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller, S., Dykes, D. and Polesky, H. (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res., 16, 1215.
-
(1988)
Nucleic Acids Res.
, vol.16
, pp. 1215
-
-
Miller, S.1
Dykes, D.2
Polesky, H.3
-
56
-
-
26144438528
-
Statistically significant association of sequence variants in the ABCR gene with age-related macular degeneration
-
Allikmets, R. and the International ABCR Screening Consortium (1999) Statistically significant association of sequence variants in the ABCR gene with age-related macular degeneration. Am. J. Hum. Genet., 65, A103.
-
(1999)
Am. J. Hum. Genet.
, vol.65
-
-
Allikmets, R.1
-
57
-
-
0032231941
-
PedCheck: A program for identifying genotype incompatibilities in linkage analysis
-
O'Connell, J.R. and Weeks, D.E. (1998) PedCheck: a program for identifying genotype incompatibilities in linkage analysis. Am. J. Hum. Genet., 63, 259-266.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 259-266
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
58
-
-
0023894935
-
The affected-pedigree-member method of linkage analysis
-
Weeks, D. and Lange, K. (1988) The affected-pedigree-member method of linkage analysis. Am. J. Hum. Genet., 42, 315-326.
-
(1988)
Am. J. Hum. Genet.
, vol.42
, pp. 315-326
-
-
Weeks, D.1
Lange, K.2
-
59
-
-
0029945706
-
Descent graphs in pedigree analysis: Applications to haplotyping, location scores and marker-sharing statistics
-
Sobel, E. and Lange, K. (1996) Descent graphs in pedigree analysis: applications to haplotyping, location scores and marker-sharing statistics. Am. J. Hum. Genet., 58, 1323-1337.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 1323-1337
-
-
Sobel, E.1
Lange, K.2
-
60
-
-
0030881661
-
Accurate inference of relationships in sib-pair linkage studies
-
Boehnke, M. and Cox, N.J. (1997) Accurate inference of relationships in sib-pair linkage studies. Am. J. Hum. Genet., 61, 423-429.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 423-429
-
-
Boehnke, M.1
Cox, N.J.2
-
61
-
-
0025964920
-
Allele frequency estimation from data on relatives
-
Boehnke, M. (1991) Allele frequency estimation from data on relatives. Am. J. Hum. Genet., 48, 22-25.
-
(1991)
Am. J. Hum. Genet.
, vol.48
, pp. 22-25
-
-
Boehnke, M.1
-
62
-
-
0026629701
-
Strategies for characterizing highly polymorphic markers in human gene mapping
-
Ott, J. (1992) Strategies for characterizing highly polymorphic markers in human gene mapping. Am. J. Hum. Genet., 51, 283-290.
-
(1992)
Am. J. Hum. Genet.
, vol.51
, pp. 283-290
-
-
Ott, J.1
-
63
-
-
0034164617
-
Linkage analysis in the presence of errors III: Marker loci and their map as nuisance parameters
-
Göring, H.H.H. and Terwilliger, J.D. (2000) Linkage analysis in the presence of errors III: Marker loci and their map as nuisance parameters. Am. J. Hum. Genet., 66, 1298-1309.
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 1298-1309
-
-
Göring, H.H.H.1
Terwilliger, J.D.2
-
64
-
-
0021070232
-
The search for heterogeneity in insulin-dependent diabetes mellitus (IDDM): Linkage studies, two-locus models and genetic heterogeneity
-
Hodge, S.E., Anderson, C.E., Neiswanger, K., Sparkes, R.S. and Rimoin, D.L. (1983) The search for heterogeneity in insulin-dependent diabetes mellitus (IDDM): linkage studies, two-locus models and genetic heterogeneity. Am. J. Hum. Genet., 5, 1139-1155.
-
(1983)
Am. J. Hum. Genet.
, vol.5
, pp. 1139-1155
-
-
Hodge, S.E.1
Anderson, C.E.2
Neiswanger, K.3
Sparkes, R.S.4
Rimoin, D.L.5
-
65
-
-
0023933932
-
Efficient computations in multilocus linkage analysis
-
Lathrop, G.M. and Lalouel, J.M. (1988) Efficient computations in multilocus linkage analysis. Am. J. Hum. Genet., 42, 498-505.
-
(1988)
Am. J. Hum. Genet.
, vol.42
, pp. 498-505
-
-
Lathrop, G.M.1
Lalouel, J.M.2
-
66
-
-
0342499587
-
Strategies for multilocus linkage analysis in humans
-
Lathrop, G.M., Lalouel, J.M., Julier, C. and Ott, J. (1984) Strategies for multilocus linkage analysis in humans. Proc. Natl Acad. Sci. USA, 81, 3443-3446.
-
(1984)
Proc. Natl Acad. Sci. USA
, vol.81
, pp. 3443-3446
-
-
Lathrop, G.M.1
Lalouel, J.M.2
Julier, C.3
Ott, J.4
-
67
-
-
0027366195
-
Faster sequential genetic linkage computations
-
Cottingham, R.W., Idury, R.M. and Schäffer, A.A. (1993) Faster sequential genetic linkage computations. Am. J. Hum. Genet., 53, 252-263.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 252-263
-
-
Cottingham, R.W.1
Idury, R.M.2
Schäffer, A.A.3
-
68
-
-
0028260703
-
Avoiding recomputation in linkage analysis
-
Schäffer, A.A., Gupta, S.K., Shriram, K. and Cottingham, R.W. (1994) Avoiding recomputation in linkage analysis. Hum. Hered., 44, 225-237.
-
(1994)
Hum. Hered.
, vol.44
, pp. 225-237
-
-
Schäffer, A.A.1
Gupta, S.K.2
Shriram, K.3
Cottingham, R.W.4
-
69
-
-
0029946879
-
Faster linkage analysis computations for pedigrees with loops or unused alleles
-
Schäffer, A.A. (1996) Faster linkage analysis computations for pedigrees with loops or unused alleles. Hum. Hered., 46, 226-235.
-
(1996)
Hum. Hered.
, vol.46
, pp. 226-235
-
-
Schäffer, A.A.1
-
70
-
-
0022919732
-
Linkage probability and its approximate confidence interval under possible heterogeneity
-
Ott, J. (1986) Linkage probability and its approximate confidence interval under possible heterogeneity. Genet. Epidemiol., Suppl. 1, 251-257.
-
(1986)
Genet. Epidemiol., Suppl.
, vol.1
, pp. 251-257
-
-
Ott, J.1
-
71
-
-
0029886532
-
Parametric and nonparametric linkage analysis: A unified multipoint approach
-
Kruglyak, L., Daly, M.J., Reeve-Daly, M.P. and Lander, E.S. (1996) Parametric and nonparametric linkage analysis: a unified multipoint approach. Am. J. Hum. Genet., 58, 1347-1363.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 1347-1363
-
-
Kruglyak, L.1
Daly, M.J.2
Reeve-Daly, M.P.3
Lander, E.S.4
-
72
-
-
0029918883
-
Nonparametric simulation-based statistics for detecting linkage in general pedigrees
-
Davis, S., Schroeder, M., Goldin, L.R. and Weeks, D.E. (1996) Nonparametric simulation-based statistics for detecting linkage in general pedigrees. Am. J. Hum. Genet., 58, 867-880.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 867-880
-
-
Davis, S.1
Schroeder, M.2
Goldin, L.R.3
Weeks, D.E.4
-
73
-
-
26144480880
-
Improvements to SimIBD, a nonparametric method for detecting linkage in general pedigrees
-
Davis, S. and Weeks, D.E. (1997) Improvements to SimIBD, a nonparametric method for detecting linkage in general pedigrees. Am. J. Hum. Genet., 61 (suppl.), A272.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, Issue.SUPPL.
-
-
Davis, S.1
Weeks, D.E.2
-
74
-
-
0001261886
-
SimIBD: A powerful robust nonparametric method for detecting linkage in general pedigrees
-
Pawlowitzki, I.H., Edwards, J.H. and Thompson, E.A. (eds)
-
Davis, S., Goldin, L.R. and Weeks, D.E. (1997) SimIBD: a powerful robust nonparametric method for detecting linkage in general pedigrees. In Pawlowitzki, I.H., Edwards, J.H. and Thompson, E.A. (eds), Genetic Mapping of Disease Genes. Academic Press, London, UK, pp. 189-204.
-
(1997)
Genetic Mapping of Disease Genes. Academic Press, London, UK
, pp. 189-204
-
-
Davis, S.1
Goldin, L.R.2
Weeks, D.E.3
-
75
-
-
0030728925
-
Allele-sharing models: LOD scores and accurate linkage tests
-
Kong, A. and Cox, N.J. (1997) Allele-sharing models: LOD scores and accurate linkage tests. Am. J. Hum. Genet., 61, 1179-1188.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 1179-1188
-
-
Kong, A.1
Cox, N.J.2
-
77
-
-
0039513062
-
Computer-simulation methods in human linkage analysis
-
Ott, J. (1989) Computer-simulation methods in human linkage analysis. Proc. Natl Acad. Sci. USA, 86, 4175-1178.
-
(1989)
Proc. Natl Acad. Sci. USA
, vol.86
, pp. 4175-11178
-
-
Ott, J.1
-
78
-
-
0000801438
-
SLINK: A general simulation program for linkage analysis
-
Weeks, D.E., Ott, J. and Lathrop, G.M. (1990) SLINK: a general simulation program for linkage analysis. Am. J. Hum. Genet., 47, A204.
-
(1990)
Am. J. Hum. Genet.
, vol.47
-
-
Weeks, D.E.1
Ott, J.2
Lathrop, G.M.3
-
79
-
-
0027213849
-
Chromosome-based method for rapid computer simulation in human genetic linkage analysis
-
Terwilliger, J.D., Speer, M. and Ott, J. (1993) Chromosome-based method for rapid computer simulation in human genetic linkage analysis. Genet. Epidemiol., 10, 217-224.
-
(1993)
Genet. Epidemiol.
, vol.10
, pp. 217-224
-
-
Terwilliger, J.D.1
Speer, M.2
Ott, J.3
-
80
-
-
0027372405
-
A gene for Stargardt's disease (fundus flavimaculatus) maps to the short arm of chromosome 1
-
Kaplan, J., Gerber, S., Larget-Piet, D., Rozet, J.M., Dollfus, H., Dufier, J.L., Odent, S., Postel-Vinay, A., Janin, N., Briard, M.L. et al. (1993) A gene for Stargardt's disease (fundus flavimaculatus) maps to the short arm of chromosome 1. Nature Genet., 5, 308-311.
-
(1993)
Nature Genet.
, vol.5
, pp. 308-311
-
-
Kaplan, J.1
Gerber, S.2
Larget-Piet, D.3
Rozet, J.M.4
Dollfus, H.5
Dufier, J.L.6
Odent, S.7
Postel-Vinay, A.8
Janin, N.9
Briard, M.L.10
-
81
-
-
9044250844
-
Linkage of autosomal dominant radial drusen (Malattia Leventinese) to chromosome 2p16-21
-
Heon, E., Piguet, B., Munier, F., Sneed, S.R., Morgan, C.M., Forni, S., Grasiano, P., Schorderet, D., Taylor, C.M., Streb, L.M., Wiles, C.D., Nishimura, D. Y., Sheffield, V.C. and Stone, E.M. (1996) Linkage of autosomal dominant radial drusen (Malattia Leventinese) to chromosome 2p16-21. Arch. Ophthalmol., 114, 193-198.
-
(1996)
Arch. Ophthalmol.
, vol.114
, pp. 193-198
-
-
Heon, E.1
Piguet, B.2
Munier, F.3
Sneed, S.R.4
Morgan, C.M.5
Forni, S.6
Grasiano, P.7
Schorderet, D.8
Taylor, C.M.9
Streb, L.M.10
Wiles, C.D.11
Nishimura, D.Y.12
Sheffield, V.C.13
Stone, E.M.14
-
82
-
-
0025105161
-
A point mutation of the rhodopsin gene in one form of retinitis pigmentosa
-
Dryja, T., McGee, T., Reichel, E., Hahn, L., Cowley, G., Yandell, D., Sandberg, M. and Berson, E. (1990) A point mutation of the rhodopsin gene in one form of retinitis pigmentosa. Nature, 343, 364-366.
-
(1990)
Nature
, vol.343
, pp. 364-366
-
-
Dryja, T.1
McGee, T.2
Reichel, E.3
Hahn, L.4
Cowley, G.5
Yandell, D.6
Sandberg, M.7
Berson, E.8
-
83
-
-
0025720710
-
Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa
-
Kajiwara, K., Hahn, L.B., Mukai, S., Travis, G.H., Berson, E.L. and Dryja, T.P. (1991) Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. Nature, 354, 480-483.
-
(1991)
Nature
, vol.354
, pp. 480-483
-
-
Kajiwara, K.1
Hahn, L.B.2
Mukai, S.3
Travis, G.H.4
Berson, E.L.5
Dryja, T.P.6
-
84
-
-
0026710901
-
North Carolina macular dystrophy is assigned to chromosome 6
-
Small, K.W., Weber, J.L., Roses, A., Lennon, F., Vance, J.M. and Pericak-Vance, M.A. (1992) North Carolina macular dystrophy is assigned to chromosome 6. Genomics, 13, 681-685.
-
(1992)
Genomics
, vol.13
, pp. 681-685
-
-
Small, K.W.1
Weber, J.L.2
Roses, A.3
Lennon, F.4
Vance, J.M.5
Pericak-Vance, M.A.6
-
85
-
-
0027309259
-
A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p
-
Inglehearn, C.F., Carter, S.A., Keen, T.J., Lindsey, J., Stephenson, A.M., Bashir, R., al-Maghtheh, M., Moore, A.T., Jay, M., Bird, A.C. et al. (1993) A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p. Nature Genet., 4, 51-53.
-
(1993)
Nature Genet.
, vol.4
, pp. 51-53
-
-
Inglehearn, C.F.1
Carter, S.A.2
Keen, T.J.3
Lindsey, J.4
Stephenson, A.M.5
Bashir, R.6
Al-Maghtheh, M.7
Moore, A.T.8
Jay, M.9
Bird, A.C.10
-
86
-
-
0027155177
-
Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q
-
Jordan, S.A., Farrar, G.J., Kenna, P., Humphries, M.M., Sheils, D.M., Kumar-Singh, R., Sharp, E.M., Soriano, N., Ayuso, C., Benitez, J. et al. (1993) Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q. Nature Genet., 4, 54-58.
-
(1993)
Nature Genet.
, vol.4
, pp. 54-58
-
-
Jordan, S.A.1
Farrar, G.J.2
Kenna, P.3
Humphries, M.M.4
Sheils, D.M.5
Kumar-Singh, R.6
Sharp, E.M.7
Soriano, N.8
Ayuso, C.9
Benitez, J.10
-
87
-
-
0026347736
-
Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8
-
Blanton, S.H., Heckenlively, J.R., Cottingham, A.W., Friedman, J., Sadler, L.A., Wagner, M., Friedman, L.H. and Daiger, S.P. (1991) Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8. Genomics, 11, 857-869.
-
(1991)
Genomics
, vol.11
, pp. 857-869
-
-
Blanton, S.H.1
Heckenlively, J.R.2
Cottingham, A.W.3
Friedman, J.4
Sadler, L.A.5
Wagner, M.6
Friedman, L.H.7
Daiger, S.P.8
-
88
-
-
0028237047
-
The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8
-
Tahvanainen, E., Ranta, S., Hirvasniemi, A., Karila, E., Leisti, J., Sistonen, P., Weissenbach, J., Lehesjoki, A.E. and de la Chapelle, A. (1994) The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8. Proc. Natl Acad. Sci. USA, 91, 7267-7270.
-
(1994)
Proc. Natl Acad. Sci. USA
, vol.91
, pp. 7267-7270
-
-
Tahvanainen, E.1
Ranta, S.2
Hirvasniemi, A.3
Karila, E.4
Leisti, J.5
Sistonen, P.6
Weissenbach, J.7
Lehesjoki, A.E.8
De La Chapelle, A.9
-
89
-
-
0026895234
-
Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13
-
Stone, E.M., Nichols, B.E., Streb, L., Kimura, A.E. and Sheffield, V.C. (1992) Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13. Nature Genet., 1, 246-250.
-
(1992)
Nature Genet.
, vol.1
, pp. 246-250
-
-
Stone, E.M.1
Nichols, B.E.2
Streb, L.3
Kimura, A.E.4
Sheffield, V.C.5
-
90
-
-
0027058412
-
Linkage of Usher syndrome type I gene (USHIB) to the long arm of chromosome 11
-
Kimberling, W.J., Moller, C.G., Davenport, S., Priluck, I.A., Beighton, P.H., Greenberg, J., Reardon, W., Weston, M.D., Kenyon, J.B., Grunkemeyer, J.A. et al. (1992) Linkage of Usher syndrome type I gene (USHIB) to the long arm of chromosome 11. Genomics, 14, 988-994.
-
(1992)
Genomics
, vol.14
, pp. 988-994
-
-
Kimberling, W.J.1
Moller, C.G.2
Davenport, S.3
Priluck, I.A.4
Beighton, P.H.5
Greenberg, J.6
Reardon, W.7
Weston, M.D.8
Kenyon, J.B.9
Grunkemeyer, J.A.10
-
91
-
-
0028366078
-
A dominant Stargardt's macular dystrophy locus maps to chromosome 13q34
-
Zhang, K., Bither, P.P., Park, R., Donoso, L.A., Seidman, J.G. and Seidman, C.E. (1994) A dominant Stargardt's macular dystrophy locus maps to chromosome 13q34. Arch. Ophthalmol., 112, 759-764.
-
(1994)
Arch. Ophthalmol.
, vol.112
, pp. 759-764
-
-
Zhang, K.1
Bither, P.P.2
Park, R.3
Donoso, L.A.4
Seidman, J.G.5
Seidman, C.E.6
-
92
-
-
0027058632
-
A gene for Usher syndrome type I (USHIA) maps to chromosome 14q
-
Kaplan, J., Gerber, S., Bonneau, D., Rozet, J.M., Delrieu, O., Briard, M.L., Dollfus, H., Ghazi, I., Dufier, J.L., Frezal, J. et al. (1992) A gene for Usher syndrome type I (USHIA) maps to chromosome 14q. Genomics, 14, 979-987.
-
(1992)
Genomics
, vol.14
, pp. 979-987
-
-
Kaplan, J.1
Gerber, S.2
Bonneau, D.3
Rozet, J.M.4
Delrieu, O.5
Briard, M.L.6
Dollfus, H.7
Ghazi, I.8
Dufier, J.L.9
Frezal, J.10
-
93
-
-
0028244138
-
Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion
-
Evans, K., Fryer, A., Inglehearn, C., Duvall-Young, J., Whittaker, J.L., Gregory, C.Y., Butler, R., Ebenezer, N., Hunt, D.M. and Bhattacharya, S. (1994) Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion. Nature Genet., 6, 210-213.
-
(1994)
Nature Genet.
, vol.6
, pp. 210-213
-
-
Evans, K.1
Fryer, A.2
Inglehearn, C.3
Duvall-Young, J.4
Whittaker, J.L.5
Gregory, C.Y.6
Butler, R.7
Ebenezer, N.8
Hunt, D.M.9
Bhattacharya, S.10
-
94
-
-
0028304097
-
Sorsby's fundus dystrophy is genetically linked to chromosome 22q13-qter
-
Weber, B.H., Vogt. G., Wolz, W., Ives, E.J. and Ewing, C.C. (1994) Sorsby's fundus dystrophy is genetically linked to chromosome 22q13-qter. Nature Genet., 7, 158-161.
-
(1994)
Nature Genet.
, vol.7
, pp. 158-161
-
-
Weber, B.H.1
Vogt, G.2
Wolz, W.3
Ives, E.J.4
Ewing, C.C.5
|