-
1
-
-
0025368589
-
Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents
-
Albertsen, H.M., H. Abderrahim, H.M. Cann, J. Dausset, D. Le Paslier, and D. Cohen. 1990. Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents. Proc. Natl. Acad. Sci. 87: 4256-4260.
-
(1990)
Proc. Natl. Acad. Sci.
, vol.87
, pp. 4256-4260
-
-
Albertsen, H.M.1
Abderrahim, H.2
Cann, H.M.3
Dausset, J.4
Le Paslier, D.5
Cohen, D.6
-
2
-
-
0025183708
-
Basic local alignment search tool
-
Altschul, S.F., W. Gish, W. Miller, E.W. Myers, and D.J. Lipman. 1990. Basic local alignment search tool. J. Mol. Biol. 215: 403-410.
-
(1990)
J. Mol. Biol.
, vol.215
, pp. 403-410
-
-
Altschul, S.F.1
Gish, W.2
Miller, W.3
Myers, E.W.4
Lipman, D.J.5
-
3
-
-
0025369509
-
A 3.5 genome equivalent multi access YAC library: Construction, characterization, screening and storage
-
Anand, R., J.H. Riley, R. Butler, J.C. Smith, and A.F. Markham. 1990. A 3.5 genome equivalent multi access YAC library: Construction, characterization, screening and storage. Nucleic Acids Res. 18: 1951-1956.
-
(1990)
Nucleic Acids Res.
, vol.18
, pp. 1951-1956
-
-
Anand, R.1
Riley, J.H.2
Butler, R.3
Smith, J.C.4
Markham, A.F.5
-
5
-
-
9844242745
-
-
Ayyagari, R., R.J.H. Smith, M. Polymeropoulos, A.C. Chinault, S.P. Daiger, M.Z. Pelias, L. Wozencraft, M. Kaiser-Kupfer, and J.F. Hejtmancik. 1994. Invest. Ophthalmol.Vis. Sci. (Abstr.) 35: 2143.
-
(1994)
Invest. Ophthalmol.Vis. Sci. (Abstr.)
, vol.35
, pp. 2143
-
-
Ayyagari, R.1
Smith, R.J.H.2
Polymeropoulos, M.3
Chinault, A.C.4
Daiger, S.P.5
Pelias, M.Z.6
Wozencraft, L.7
Kaiser-Kupfer, M.8
Hejtmancik, J.F.9
-
6
-
-
0029652147
-
Fine mapping of Usher syndrome type 1C to chromosome 11p14 and identification of flanking markers by haplotype analysis
-
Ayyagari, R., Y. Li, R.J.H. Smith, M.Z. Pelias, and J.F. Hejtmancik. 1995. Fine mapping of Usher syndrome type 1C to chromosome 11p14 and identification of flanking markers by haplotype analysis. Mol. Vision 1: 95002.
-
(1995)
Mol. Vision
, vol.1
, pp. 95002
-
-
Ayyagari, R.1
Li, Y.2
Smith, R.J.H.3
Pelias, M.Z.4
Hejtmancik, J.F.5
-
7
-
-
0024370486
-
Isolation of single-copy human genes from a library of yeast artificial chromosome clones
-
Brownstein, B.H., G.A. Silverman, R.D. Little, D.T. Burke, S.J. Korsmeyer, D. Schlessinger, and M.V. Olson. 1989. Isolation of single-copy human genes from a library of yeast artificial chromosome clones. Science 244: 1348-1351.
-
(1989)
Science
, vol.244
, pp. 1348-1351
-
-
Brownstein, B.H.1
Silverman, G.A.2
Little, R.D.3
Burke, D.T.4
Korsmeyer, S.J.5
Schlessinger, D.6
Olson, M.V.7
-
8
-
-
0000852818
-
-
ed. M. Burmeister and I. Ulanovsky, The Humana Press Inc., Totowa, N.J.
-
Chandrasekharappa, S.C., D.A. Marchuk, and F.S. Collins. 1992. In Methods in Molecular Biology (ed. M. Burmeister and I. Ulanovsky), pp. 235-257. The Humana Press Inc., Totowa, N.J.
-
(1992)
Methods in Molecular Biology
, pp. 235-257
-
-
Chandrasekharappa, S.C.1
Marchuk, D.A.2
Collins, F.S.3
-
9
-
-
0029653653
-
A YAC contig map of the human genome
-
Chumakov, I.M., P. Rigault, I. Le Gall, C. Bellane-Chantelot, A. Billault, S. Guillou, P. Soularue, G. Guasconi, E. Pouillier, I. Gros, et al. 1995. A YAC contig map of the human genome. Nature (Suppl.) 377: 175-299.
-
(1995)
Nature (Suppl.)
, vol.377
, pp. 175-299
-
-
Chumakov, I.M.1
Rigault, P.2
Le Gall, I.3
Bellane-Chantelot, C.4
Billault, A.5
Guillou, S.6
Soularue, P.7
Guasconi, G.8
Pouillier, E.9
Gros, I.10
-
10
-
-
0027723477
-
A first-generation physical map of the human genome
-
Cohen, D., I. Chumakov, and J. Weissenbach. 1993. A first-generation physical map of the human genome. Nature 366: 698-701.
-
(1993)
Nature
, vol.366
, pp. 698-701
-
-
Cohen, D.1
Chumakov, I.2
Weissenbach, J.3
-
11
-
-
0029021696
-
Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy
-
Thomas, P.M., G.J. Cote, N. Wohlik, B. Haddad, P.M. Mathew, W. Rabl, L. Aguilar-Bryan, R.F. Gagel, and J. Bryan. 1995b. Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy. Science 268: 426-429.
-
(1995)
Science
, vol.268
, pp. 426-429
-
-
Thomas, P.M.1
Cote, G.J.2
Wohlik, N.3
Haddad, B.4
Mathew, P.M.5
Rabl, W.6
Aguilar-Bryan, L.7
Gagel, R.F.8
Bryan, J.9
-
12
-
-
0028815440
-
Defective myosin VIIA gene responsible for Usher syndrome type IB
-
Weil, D., S. Blanchard, J. Kaplan, P. Guilford, F. Gibson, J. Walsh, P. Mburu, A. Varela, J. Levilliers, and M.D. Weston. 1995. Defective myosin VIIA gene responsible for Usher syndrome type IB. Nature 374: 60-61.
-
(1995)
Nature
, vol.374
, pp. 60-61
-
-
Weil, D.1
Blanchard, S.2
Kaplan, J.3
Guilford, P.4
Gibson, F.5
Walsh, J.6
Mburu, P.7
Varela, A.8
Levilliers, J.9
Weston, M.D.10
-
13
-
-
0026446099
-
A second-generation linkage map of the human genome
-
Weissenbach, J., G. Gyapay, C. Dib, A. Vignal, J. Morissette, P. Millaseau, G. Vaysseix, and M. Lathrop. 1992. A second-generation linkage map of the human genome. Nature 359: 794-801.
-
(1992)
Nature
, vol.359
, pp. 794-801
-
-
Weissenbach, J.1
Gyapay, G.2
Dib, C.3
Vignal, A.4
Morissette, J.5
Millaseau, P.6
Vaysseix, G.7
Lathrop, M.8
-
14
-
-
19144370283
-
-
Whitehead Institute/MIT Center for Genome Research, Human Genetic Mapping Project. 1995. Data release 8
-
Whitehead Institute/MIT Center for Genome Research, Human Genetic Mapping Project. 1995. Data release 8.
-
-
-
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