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Results 1-10 of 18 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
1997A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndromeMuenke, M.; Gripp, K.; McDonald-McGinn, D.; Gaudenz, K.; Whitaker, L.; Bartlett, S.; Markowitz, R.; Robin, N.; Nwokoro, N.; Mulvihill, J.; Losken, H.; Mulliken, J.; Guttmacher, A.; Wilroy, R.; Clarke, L.; Hollway, G.; Ades, L.; Haan, E.; Mulley, J.; Cohen, M.; et al.
1995An integrated physical map of human chromosome 16Doggett, N.; Goodwin, L.; Tesmer, J.; Meincke, L.; Bruce, D.; Clark, L.; Altherr, M.; Ford, A.; Chi, H.; Marrone, B.; Longmire, J.; Lane, S.; Whitmore, S.; Lowenstein, N.; Sutherland, G.; Mundt, M.; Knill, E.; Bruno, W.; Macken, C.; Torney, D.; et al.
1999TeV gamma-ray observations of three X-ray selected BL LacsRoberts, M.; McGee, P.; Dazeley, S.; Edwards, P.; Hara, T.; Holder, J.; Kawachi, A.; Kifune, T.; Matsubara, Y.; Mizumoto, Y.; Mori, M.; Muraishi, H.; Muraki, Y.; Naito, T.; Nishijima, K.; Ogio, S.; Osaki, T.; Patterson, J.; Rowell, G.; Sako, T.; et al.
1998Discovery of TeV Gamma Rays from SN 1006: Further Evidence for the Supernova Remnant Origin of Cosmic RaysTanimori, T.; Hayami, Y.; Kamei, S.; Dazeley, S.; Edwards, P.; Roberts, M.; Gunji, S.; Hara, S.; Hara, T.; Holder, J.; Kawachi, A.; Kifune, T.; Kita, R.; Konishi, T.; Masaike, A.; Matsubara, Y.; Matsuoka, T.; Mizumoto, Y.; Mori, M.; Moriya, M.; et al.
1999Present status of the 7-10 m telescope of CANGAROO IIYoshikoshi, T.; Dazeley, S.; Gunji, S.; Hara, S.; Hara, T.; Holder, J.; Jimbo, J.; Kawachi, A.; Kifune, T.; Kubo, H.; Kushida, J.; Bohec, S.; Matsubara, Y.; Mizumoto, Y.; Mori, M.; Moriya, M.; Muraishi, H.; Muraki, Y.; Naito, T.; Nishijima, K.; et al.
1999Geometrical reconstruction with the High Resolution Fly's Eye prototype cosmic ray detectorWilkinson, C.; Abu-Zayyad, T.; Al-Seady, M.; Belov, K.; Bird, D.; Boyer, J.; Chen, G.; Clay, R.; Dai, H.; Dawson, B.; Ho, Y.; Huang, M.; Jui, C.; Kidd, M.; Kieda, D.; Knapp, B.; Lee, W.; Loh, E.; Mannel, E.; Matthews, J.; et al.
1998TeV gamma-ray observations of three southern BL Lacs with the CANGAROO 3.8m Imaging TelescopeRoberts, M.; Dazeley, S.; Edwards, P.; Hara, T.; Hayami, Y.; Holder, J.; Kakimoto, F.; Kamei, S.; Kawachi, A.; Kifune, T.; Kita, R.; Konishi, T.; Masaike, A.; Matsubara, Y.; Matsuoka, T.; Mizumoto, Y.; Mori, M.; Muraishi, H.; Muraki, Y.; Nishijima, K.; et al.
1999Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromesMcDermott, M.; Aksentijevich, I.; Galon, J.; McDermott, E.; Ogunkolade, B.; Centola, M.; Mansfield, E.; Gadina, M.; Karenko, L.; Petterson, T.; McCarthy, J.; Frucht, D.; Aringer, M.; Torosyan, Y.; Teppo, A.; Wilson, M.; Karaarslan, H.; Wan, Y.; Todd, I.; Wood, G.; et al.
1997Ancient missense mutations in a new member of the RoRet gene family are likely to cause Familial Mediterranean FeverAksentijevich, I.; Centola, M.; Deng, Z.; Sood, R.; Balow, J.; Wood, G.; Zaks, N.; Mansfield, E.; Chen, X.; Eisenberg, S.; Vedula, A.; Shafran, N.; Raben, N.; Pras, E.; Pras, M.; Kastner, D.; Blake, T.; Baxevanis, A.; Robbins, C.; Krizman, D.; et al.
1997Construction of a 1-Mb restriction-mapped cosmid contig containing the candidate region for the Familial Mediterranean Fever Locus (MEFV) on chromosome 16p13.3Sood, R.; Blake, T.; Aksentijevich, I.; Wood, G.; Chen, X.; Gardner, D.; Shelton, D.; Mangelsdorf, M.; Orsborn, A.; Pras, E.; Balow, J.; Centola, M.; Deng, Z.; Zaks, N.; Chen, X.; Richards, N.; Fischel-Ghodsian, N.; Rotter, J.; Pras, M.; Shohat, M.; et al.