-
2
-
-
0025965687
-
Signs, complications, and platelet aggregation in familial exudative vitreoretinopathy
-
Van Nouhuys CE. Signs, complications, and platelet aggregation in familial exudative vitreoretinopathy. Am J Ophthalmol 1991;111:34-41.
-
(1991)
Am J Ophthalmol
, vol.111
, pp. 34-41
-
-
Van Nouhuys, C.E.1
-
3
-
-
0027212143
-
Familial exudative vitreoretinopathy
-
Ebert EM, Mukai S. Familial exudative vitreoretinopathy. Int Ophthalmol Clin 1993;33:237-47.
-
(1993)
Int Ophthalmol Clin
, vol.33
, pp. 237-247
-
-
Ebert, E.M.1
Mukai, S.2
-
4
-
-
0002988313
-
-
Berson EL, D'Amico DJ, Schepens CL, eds. Philadelphia: Saunders
-
Mukai S, Mukai E, Puliafito CA, In: Berson EL, D'Amico DJ, Schepens CL, eds. Principles and practice of ophthalmology. Philadelphia: Saunders, 1994:813-17.
-
(1994)
Principles and Practice of Ophthalmology
, pp. 813-817
-
-
Mukai, S.1
Mukai, E.2
Puliafito, C.A.3
-
5
-
-
0020321381
-
Retinal involvement in familial exudative vitreoretinopathy
-
Miyakubo H, Inohara N, Hashimoto K. Retinal involvement in familial exudative vitreoretinopathy. Ophthalmologica 1982;185:125-35.
-
(1982)
Ophthalmologica
, vol.185
, pp. 125-135
-
-
Miyakubo, H.1
Inohara, N.2
Hashimoto, K.3
-
6
-
-
0017051492
-
Fluorescein angiographic findings in familial exudative vitreoretinopathy
-
Canny CL, Oliver GL. Fluorescein angiographic findings in familial exudative vitreoretinopathy. Arch Ophthalmol 1976;94:1114-20.
-
(1976)
Arch Ophthalmol
, vol.94
, pp. 1114-1120
-
-
Canny, C.L.1
Oliver, G.L.2
-
8
-
-
0018347279
-
Familial exudative vitreoretinopathy
-
Slusher MM, Hutton WE. Familial exudative vitreoretinopathy. Am J Ophthalmol 1979;87:152-6.
-
(1979)
Am J Ophthalmol
, vol.87
, pp. 152-156
-
-
Slusher, M.M.1
Hutton, W.E.2
-
9
-
-
0034622122
-
A brief review of retinitis pigmentosa and the identified retinitis pigmentosa genes
-
Phelan JK, Bok D. A brief review of retinitis pigmentosa and the identified retinitis pigmentosa genes. Mol Vis 2000;6:116-24.
-
(2000)
Mol Vis
, vol.6
, pp. 116-124
-
-
Phelan, J.K.1
Bok, D.2
-
10
-
-
0031575703
-
Familial exudative vitreoretinopathy: Further evidence for genetic heterogeneity
-
Shastry BS, Trese MT. Familial exudative vitreoretinopathy: further evidence for genetic heterogeneity. Am J Med Genet 1997;69:217-18.
-
(1997)
Am J Med Genet
, vol.69
, pp. 217-218
-
-
Shastry, B.S.1
Trese, M.T.2
-
11
-
-
14444268540
-
Autosomal recessive familial exudative vitreoretinopathy: Evidence for genetic heterogeneity
-
De Crecchio G, Simonelli F, Nunziata G, et al. Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity. Clin Genet 1998;54:315-20.
-
(1998)
Clin Genet
, vol.54
, pp. 315-320
-
-
De Crecchio, G.1
Simonelli, F.2
Nunziata, G.3
-
12
-
-
0030902358
-
Identification of novel missense mutations in the Norrie disease gene associated with one X-linked and four sporadic cases of familial exudative vitreoretinopathy
-
Shastry BS, Hejtmancik JF, Trese MT. Identification of novel missense mutations in the Norrie disease gene associated with one X-linked and four sporadic cases of familial exudative vitreoretinopathy. Hum Mutat 1997;9:396-401.
-
(1997)
Hum Mutat
, vol.9
, pp. 396-401
-
-
Shastry, B.S.1
Hejtmancik, J.F.2
Trese, M.T.3
-
13
-
-
0026728482
-
The gene for autosomal dominant familial exudative vitreoretinopathy (Criswick-Schepens) on the long arm of chromosome 11
-
Li Y, Fuhrmann C, Schwinger E, et al. The gene for autosomal dominant familial exudative vitreoretinopathy (Criswick-Schepens) on the long arm of chromosome 11. Am J Ophthalmol 1992;113:712-13.
-
(1992)
Am J Ophthalmol
, vol.113
, pp. 712-713
-
-
Li, Y.1
Fuhrmann, C.2
Schwinger, E.3
-
14
-
-
0028280907
-
Mapping of the autosomal dominant exudative vitreoretinopathy locus (EVR1) by multipoint linkage analysis in four families
-
Muller B, van Nouhuys CE, Duvigneau C, et al. Mapping of the autosomal dominant exudative vitreoretinopathy locus (EVR1) by multipoint linkage analysis in four families. Genomics 1994;20:317-19.
-
(1994)
Genomics
, vol.20
, pp. 317-319
-
-
Muller, B.1
Van Nouhuys, C.E.2
Duvigneau, C.3
-
15
-
-
0035092388
-
A new locus for autosomal dominant familial exudative vitreoretinopathy maps to chromosome 11 p12-13
-
Downey LM, Keen TJ, Roberts E, et al. A new locus for autosomal dominant familial exudative vitreoretinopathy maps to chromosome 11 p12-13. Am J Hum Genet 2001;68:778-81.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 778-781
-
-
Downey, L.M.1
Keen, T.J.2
Roberts, E.3
-
16
-
-
0027367772
-
A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy
-
Chen ZY, Battinelli EM, Fielder A, et al. A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy. Nat Genet 1993;5:180-3.
-
(1993)
Nat Genet
, vol.5
, pp. 180-183
-
-
Chen, Z.Y.1
Battinelli, E.M.2
Fielder, A.3
-
17
-
-
0036789449
-
Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy
-
Robitaille J, MacDonald ML, Kaykas A, et al. Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy. Nat Genet 2002;32:326-30.
-
(2002)
Nat Genet
, vol.32
, pp. 326-330
-
-
Robitaille, J.1
MacDonald, M.L.2
Kaykas, A.3
-
18
-
-
0035015985
-
Delineation of the critical interval for the familial exudative vitreoretinopathy gene by linkage and haplotype analysis
-
Kondo H, Ohno K, Tahira T, et al. Delineation of the critical interval for the familial exudative vitreoretinopathy gene by linkage and haplotype analysis. Hum Genet 2001;108:368-75.
-
(2001)
Hum Genet
, vol.108
, pp. 368-375
-
-
Kondo, H.1
Ohno, K.2
Tahira, T.3
-
19
-
-
0026090668
-
A rapid procedure for extracting genomic DNA from leukocytes
-
John SW, Weitzner G, Rozen R, et al. A rapid procedure for extracting genomic DNA from leukocytes. Nucleic Acids Res 1991;19:408.
-
(1991)
Nucleic Acids Res
, vol.19
, pp. 408
-
-
John, S.W.1
Weitzner, G.2
Rozen, R.3
-
20
-
-
0033786262
-
Microsatellite genotyping of post-PCR fluorescently labeled markers
-
Kondo H, Tahira T, Hayashi H, et al. Microsatellite genotyping of post-PCR fluorescently labeled markers. Biotechniques 2000;29:868-72.
-
(2000)
Biotechniques
, vol.29
, pp. 868-872
-
-
Kondo, H.1
Tahira, T.2
Hayashi, H.3
-
21
-
-
0027968068
-
CLUSTAL W: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
-
Thompson JD, Higgins DG, Gibson TJ. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res 1994;22:4673-80.
-
(1994)
Nucleic Acids Res
, vol.22
, pp. 4673-4680
-
-
Thompson, J.D.1
Higgins, D.G.2
Gibson, T.J.3
-
22
-
-
0033517824
-
Molecular cloning and characterization of human frizzled-4 on chromosome 11q14-q21
-
Kirikoshi H, Sagara N, Koike J, et al. Molecular cloning and characterization of human frizzled-4 on chromosome 11q14-q21. Biochem Biophys Res Commun 1999;264:955-61.
-
(1999)
Biochem Biophys Res Commun
, vol.264
, pp. 955-961
-
-
Kirikoshi, H.1
Sagara, N.2
Koike, J.3
-
23
-
-
0036842950
-
Detecting polymorphisms and mutations in candidate genes
-
Collins JS, Schwartz CE. Detecting polymorphisms and mutations in candidate genes. Am J Hum Genet 2002;71:1251-2.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1251-1252
-
-
Collins, J.S.1
Schwartz, C.E.2
-
24
-
-
0015106895
-
Familial exudative vitreoretinopathy. An expanded view
-
Gow J, Oliver GL. Familial exudative vitreoretinopathy. An expanded view. Arch Ophthalmol 1971;86:150-5.
-
(1971)
Arch Ophthalmol
, vol.86
, pp. 150-155
-
-
Gow, J.1
Oliver, G.L.2
|