-
1
-
-
0026719393
-
Worldwide distribution of moyamoya disease
-
Goto Y, Yonekawa Y. Worldwide distribution of moyamoya disease. Neurol Med Chir (Tokyo). 1992;32:883-886.
-
(1992)
Neurol Med Chir (Tokyo)
, vol.32
, pp. 883-886
-
-
Goto, Y.1
Yonekawa, Y.2
-
2
-
-
77956711026
-
Epidemiology of spontaneous occlusion of the circle of Willis: Results of national epidemiologic survey
-
Tokyo, Japan: Ministry of Health and Welfare Japan
-
Wakai K, Tamakoshi A, Ohno Y, Kawamura T, Ikezaki K, Fukui M. Epidemiology of spontaneous occlusion of the circle of Willis: results of national epidemiologic survey. In: The Research Committee on Spontaneous Occlusion of the Circle of Willis (Moyamoya Disease) of the Ministry of Health and Welfare Japan: Annual Report 1995. Tokyo, Japan: Ministry of Health and Welfare Japan; 1995:33-37.
-
(1995)
The Research Committee on Spontaneous Occlusion of the Circle of Willis (Moyamoya Disease) of the Ministry of Health and Welfare Japan: Annual Report 1995
, pp. 33-37
-
-
Wakai, K.1
Tamakoshi, A.2
Ohno, Y.3
Kawamura, T.4
Ikezaki, K.5
Fukui, M.6
-
4
-
-
0342705734
-
Clinical genetic study on the idiopathic occlusion of the circle of Willis
-
Tokyo, Japan: Ministry of Health and Welfare Japan
-
Osawa M, Kanai N, Kawai M, Fukuyama Y. Clinical genetic study on the idiopathic occlusion of the circle of Willis. In: The Research Committee on Spontaneous Occlusion of the Circle of Willis (Moyamoya Disease) of the Ministry of Health and Welfare Japan: Annual Report 1992. Tokyo, Japan: Ministry of Health and Welfare Japan; 1992:147-152.
-
(1992)
The Research Committee on Spontaneous Occlusion of the Circle of Willis (Moyamoya Disease) of the Ministry of Health and Welfare Japan: Annual Report 1992
, pp. 147-152
-
-
Osawa, M.1
Kanai, N.2
Kawai, M.3
Fukuyama, Y.4
-
6
-
-
0025091465
-
The neurofibromatosis type 1 gene encodes a protein related to GAP
-
Xu GF, O'Connell P, Viskochil D, Cawthon R, Robertson M, Culver M, Dunn D, Stevens J, Gesteland R, White R. The neurofibromatosis type 1 gene encodes a protein related to GAP. Cell. 1990;62:599-608.
-
(1990)
Cell
, vol.62
, pp. 599-608
-
-
Xu, G.F.1
O'Connell, P.2
Viskochil, D.3
Cawthon, R.4
Robertson, M.5
Culver, M.6
Dunn, D.7
Stevens, J.8
Gesteland, R.9
White, R.10
-
7
-
-
0029896238
-
Ocular ischemic syndrome in a child with moyamoya disease and neurofibromatosis
-
Barrall JL, Summers CG. Ocular ischemic syndrome in a child with moyamoya disease and neurofibromatosis. Surv Ophthalmol. 1996;40: 500-504.
-
(1996)
Surv Ophthalmol.
, vol.40
, pp. 500-504
-
-
Barrall, J.L.1
Summers, C.G.2
-
9
-
-
0026694404
-
Neurofibromatosis cerebral vasculopathy in an infant: Clinical, neuroradiographic, and neuropathologic studies
-
Woody RC, Perrot LJ, Beck SA. Neurofibromatosis cerebral vasculopathy in an infant: clinical, neuroradiographic, and neuropathologic studies. Pediatr Pathol. 1992;12:613-619.
-
(1992)
Pediatr Pathol.
, vol.12
, pp. 613-619
-
-
Woody, R.C.1
Perrot, L.J.2
Beck, S.A.3
-
11
-
-
0027934767
-
Familial occurrence of moyamoya disease: Magnetic resonance angiography as a screening test for high-risk subjects
-
Houkin K, Tanaka N, Takahashi A, Kamiyama H, Abe H, Kajii N. Familial occurrence of moyamoya disease: magnetic resonance angiography as a screening test for high-risk subjects. Childs Nerv Syst. 1994;10:421-425.
-
(1994)
Childs Nerv Syst.
, vol.10
, pp. 421-425
-
-
Houkin, K.1
Tanaka, N.2
Takahashi, A.3
Kamiyama, H.4
Abe, H.5
Kajii, N.6
-
12
-
-
0021850103
-
Multilocus linkage analysis in humans: Detection of linkage and estimation of recombination
-
Lathrop GM, Lalouel JM, Julier C, Ott J. Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. Am J Hum Genet. 1985;37:482-498.
-
(1985)
Am J Hum Genet.
, vol.37
, pp. 482-498
-
-
Lathrop, G.M.1
Lalouel, J.M.2
Julier, C.3
Ott, J.4
-
13
-
-
0029886532
-
Parametric and nonparametric linkage analysis: A unified multipoint approach
-
Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES. Parametric and nonparametric linkage analysis: a unified multipoint approach. Am J Hum Genet. 1996;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
-
15
-
-
0023894935
-
The affected-pedigree-member method of linkage analysis
-
Weeks DE, Lange K. The affected-pedigree-member method of linkage analysis. Am J Hum Genet. 1988;42:315-326.
-
(1988)
Am J Hum Genet.
, vol.42
, pp. 315-326
-
-
Weeks, D.E.1
Lange, K.2
-
16
-
-
0033071406
-
Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26
-
Ikeda H, Sasaki T, Yoshimoto T, Fukui M, Arinami T. Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26. Am J Hum Genet. 1999;64:533-537.
-
(1999)
Am J Hum Genet.
, vol.64
, pp. 533-537
-
-
Ikeda, H.1
Sasaki, T.2
Yoshimoto, T.3
Fukui, M.4
Arinami, T.5
-
17
-
-
0031794187
-
Mapping susceptibility genes for asthma and allergy
-
Bleecker ER. Mapping susceptibility genes for asthma and allergy. Clin Exp Allergy. 1998;28:6-12.
-
(1998)
Clin Exp Allergy
, vol.28
, pp. 6-12
-
-
Bleecker, E.R.1
-
18
-
-
0032561502
-
A physical map of 30,000 human genes
-
Deloukas P, Schuler GD, Gyapay G, Beasley EM, Soderlund C, Rodriguez-Tome P, Hui L, Matise TC, McKusick KB, Beckmann JS, Bentolila S, Bihoreau M, Birren BB, Browne J, Butler A, Castle AB, Chiannilkulchai N, Clee C, Day PJ, Dehejia A, Dibling T, Drouot N, Duprat S, Fizames C, Fox S, Gelling S, Green L, Harrison P, Hocking R, Holloway E, Hunt S, Keil S, Lijnzaad P, Louis-Dit-Sully C, Ma J, Mendis A, Miller J, Morissette J, Muselet D, Nusbaum HC, Peck A, Rozen S, Simon D, Slonim DK, Staples R, Stein LD, Stewart EA, Suchard MA, Thangarajah T, Vega-Czarny N, Webber C, Wu X, Hudson J, Auffray C, Nomura N, Sikela JM, Polymeropoulos MH, James MR, Lander ES, Hudson TJ, Myers RM, Cox DR, Weissenbach J, Boguski MS, Bentley DR. A physical map of 30,000 human genes. Science. 1998;282: 744-746.
-
(1998)
Science
, vol.282
, pp. 744-746
-
-
Deloukas, P.1
Schuler, G.D.2
Gyapay, G.3
Beasley, E.M.4
Soderlund, C.5
Rodriguez-Tome, P.6
Hui, L.7
Matise, T.C.8
McKusick, K.B.9
Beckmann, J.S.10
Bentolila, S.11
Bihoreau, M.12
Birren, B.B.13
Browne, J.14
Butler, A.15
Castle, A.B.16
Chiannilkulchai, N.17
Clee, C.18
Day, P.J.19
Dehejia, A.20
Dibling, T.21
Drouot, N.22
Duprat, S.23
Fizames, C.24
Fox, S.25
Gelling, S.26
Green, L.27
Harrison, P.28
Hocking, R.29
Holloway, E.30
Hunt, S.31
Keil, S.32
Lijnzaad, P.33
Louis-Dit-Sully, C.34
Ma, J.35
Mendis, A.36
Miller, J.37
Morissette, J.38
Muselet, D.39
Nusbaum, H.C.40
Peck, A.41
Rozen, S.42
Simon, D.43
Slonim, D.K.44
Staples, R.45
Stein, L.D.46
Stewart, E.A.47
Suchard, M.A.48
Thangarajah, T.49
Vega-Czarny, N.50
Webber, C.51
Wu, X.52
Hudson, J.53
Auffray, C.54
Nomura, N.55
Sikela, J.M.56
Polymeropoulos, M.H.57
James, M.R.58
Lander, E.S.59
Hudson, T.J.60
Myers, R.M.61
Cox, D.R.62
Weissenbach, J.63
Boguski, M.S.64
Bentley, D.R.65
more..
-
19
-
-
0027723477
-
A first-generation physical map of the human genome
-
Cohen D, Chumakov I, Weissenbach J. A first-generation physical map of the human genome. Nature. 1993;366:698-701.
-
(1993)
Nature
, vol.366
, pp. 698-701
-
-
Cohen, D.1
Chumakov, I.2
Weissenbach, J.3
-
20
-
-
0026446099
-
A second-generation linkage map of the human genome
-
Weissenbach J, Gyapay G, Dib C, Vignal A, Morissette J, Millasseau P, Vaysseix G, Lathrop M. A second-generation linkage map of the human genome. Nature. 1992;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
Millasseau, P.6
Vaysseix, G.7
Lathrop, M.8
|