-
7
-
-
0030140025
-
Localization of the gene for Cowden disease to chromosome 10q22-23
-
(1996)
Nature Genet.
, vol.13
, pp. 114-116
-
-
Nelen, M.R.1
Padberg, G.W.2
Peeters, E.A.3
Lin, A.Y.4
van den Helm, B.5
Frants, R.R.6
Coulon, V.7
Goldstein, A.M.8
van Reen, M.M.9
Easton, D.F.10
-
8
-
-
0033039497
-
Prospects for whole-genome linkage disequilibrium mapping of common disease genes
-
(1999)
Nature Genet.
, vol.22
, pp. 139-144
-
-
Kruglyak, L.1
-
12
-
-
79960655760
-
The DNA sequence of human chromosome 22
-
(1999)
Nature
, vol.402
, pp. 489-495
-
-
Dunham, I.1
Shimizu, N.2
Roe, B.A.3
Chissoe, S.4
Hunt, A.R.5
Collins, J.E.6
Bruskiewich, R.7
Beare, D.M.8
Clamp, M.9
Smink, L.J.10
-
13
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Faure, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
Millasseau, P.7
Marc, S.8
Hazan, J.9
Seboun, E.10
-
16
-
-
0031025043
-
Characterization of recombination in the HLA class II region
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 397-407
-
-
Cullen, M.1
Noble, J.2
Erlich, H.3
Thorpe, K.4
Beck, S.5
Klitz, W.6
Trowsdale, J.7
Carrington, M.8
-
17
-
-
12644260443
-
European Gene Mapping Project (EUROGEM): Breakpoint panels for human chromosomes based on the CEPH reference families. Centre d'Etude du Polymorphisme Humain
-
(1996)
Ann. Hum. Genet.
, vol.60
, pp. 447-486
-
-
Cox, S.A.1
Attwood, J.2
Bryant, S.P.3
Bains, R.4
Povey, S.5
Rebello, M.6
Kapsetaki, M.7
Moschonas, N.K.8
Grzeschik, K.H.9
Otto, M.10
-
18
-
-
0025735884
-
Linkage studies in familial Alzheimer disease: Evidence for chromosome 19 linkage
-
(1991)
Am. J. Hum. Genet.
, vol.48
, pp. 1034-1050
-
-
Pericak-Vance, M.A.1
Bebout, J.L.2
Gaskell P.C., Jr.3
Yamaoka, L.H.4
Hung, W.Y.5
Alberts, M.J.6
Walker, A.P.7
Bartlett, R.J.8
Haynes, C.A.9
Welsh, K.A.10
-
22
-
-
0032524383
-
Largescale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome
-
(1998)
Science
, vol.280
, pp. 1077-1082
-
-
Wang, D.G.1
Fan, J.-B.2
Siao, C.-J.3
Berno, A.4
Young, P.5
Sapolsky, R.6
Ghandour, G.7
Perkins, N.8
Winchester, E.9
Spencer, J.10
-
23
-
-
0033501118
-
Superiority of denaturing high performance liquid chromatography over single-stranded conformation and conformation-sensitive gel electrophoresis for mutation detection in TSC2
-
(1999)
Ann. Hum. Genet.
, vol.63
, pp. 383-391
-
-
Choy, Y.S.1
Dabora, S.L.2
Hall, F.3
Ramesh, V.4
Niida, Y.5
Franz, D.6
Kasprzyk-Obara, J.7
Reeve, M.P.8
Kwiatkowski, D.J.9
-
24
-
-
0034003411
-
Comparison of fluorescent single-strand conformation polymorphism analysis and denaturing high-performance liquid chromatography for detection of EXT1 and EXT2 mutations in hereditary multiple exostoses
-
(2000)
Eur. J. Hum. Genet.
, vol.8
, pp. 24-32
-
-
Dobson-Stone, C.1
Cox, R.D.2
Lonie, L.3
Southam, L.4
Fraser, M.5
Wise, C.6
Bernier, F.7
Hodgson, S.8
Porter, D.E.9
Simpson, A.H.10
Monaco, A.P.11
-
27
-
-
0030660620
-
Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography
-
(1997)
Genome Res.
, vol.7
, pp. 996-1005
-
-
Underhill, P.A.1
Jin, L.2
Lin, A.A.3
Mehdi, S.Q.4
Jenkins, T.5
Vollrath, D.6
Davis, R.W.7
Cavalli-Sforza, L.L.8
Oefner, P.J.9
-
28
-
-
0032529112
-
Blind analysis of denaturing high-performance liquid chromatography as a tool for mutation detection
-
(1998)
Genomics
, vol.52
, pp. 44-49
-
-
O'Donovan, M.C.1
Oefner, P.J.2
Roberts, S.C.3
Austin, J.4
Hoogendoorn, B.5
Guy, C.6
Speight, G.7
Upadhyaya, M.8
Sommer, S.S.9
McGuffin, P.10
-
29
-
-
0032990407
-
Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis
-
(1999)
Nature Genet.
, vol.22
, pp. 239-247
-
-
Halushka, M.K.1
Fan, J.B.2
Bentley, K.3
Hsie, L.4
Shen, N.5
Weder, A.6
Cooper, R.7
Lipshutz, R.8
Chakravarti, A.9
-
30
-
-
0033358728
-
Sequence diversity in 36 candidate genes for cardiovascular disorders
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 183-191
-
-
Cambien, F.1
Poirier, O.2
Nicaud, V.3
Herrmann, S.M.4
Mallet, C.5
Ricard, S.6
Behague, I.7
Hallet, V.8
Blanc, H.9
Loukaci, V.10
-
31
-
-
0034030665
-
Identification of 142 single nucleotide polymorphisms in 41 candidate genes for rheumatoid arthritis in the Japanese population
-
(2000)
Hum. Genet.
, vol.106
, pp. 293-297
-
-
Yamada, R.1
Tanaka, T.2
Ohnishi, Y.3
Suematsu, K.4
Minami, M.5
Seki, T.6
Yukioka, M.7
Maeda, A.8
Murata, N.9
Saiki, O.10
-
32
-
-
0034036664
-
Identification of 187 single nucleotide polymorphisms (SNPs) among 41 candidate genes for ischemic heart disease in the Japanese population
-
(2000)
Hum. Genet.
, vol.106
, pp. 288-292
-
-
Ohnishi, Y.1
Tanaka, T.2
Yamada, R.3
Suematsu, K.4
Minami, M.5
Fujii, K.6
Hoki, N.7
Kodama, K.8
Nagata, S.9
Hayashi, T.10
-
33
-
-
17344364213
-
DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene
-
(1998)
Nature Genet.
, vol.19
, pp. 233-240
-
-
Nickerson, D.A.1
Taylor, S.L.2
Weiss, K.M.3
Clark, A.G.4
Hutchinson, R.G.5
Stengard, J.6
Salomaa, V.7
Vartiainen, E.8
Boerwinkle, E.9
Sing, C.F.10
-
35
-
-
0032991552
-
Characterization of single-nucleotide polymorphisms in coding regions of human genes
-
(1999)
Nature Genet.
, vol.22
, pp. 231-238
-
-
Cargill, M.1
Altshuler, D.2
Ireland, J.3
Sklar, P.4
Ardlie, K.5
Patil, N.6
Shaw, N.7
Lane, C.R.8
Lim, E.P.9
Kalyanaraman, N.10
-
37
-
-
84984934752
-
Resequencing and mutational analysis using oligonucleotide microarrays
-
(1999)
Nature Genet.
, vol.21
, Issue.SUPPL. 1
, pp. 42-47
-
-
Hacia, J.G.1
-
39
-
-
0032998425
-
Polymorphism identification and quantitative detection of genomic DNA by invasive cleavage of oligonucleotide probes
-
(1999)
Nature Biotechnol.
, vol.17
, pp. 292-296
-
-
Lyamichev, V.1
Mast, A.L.2
Hall, J.G.3
Prudent, J.R.4
Kaiser, M.W.5
Takova, T.6
Kwiatkowski, R.W.7
Sander, T.J.8
de Arruda, M.9
Arco, D.A.10
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