Mislocalization of F508 CFTR in cystic fibrosis sweat glandpp321 - 327 Norbert Kartner, Olga Augustinas, Timothy J. Jensen, A. Leonard Naismith
& John R. Riordan doi:10.1038/ng0892-321 Abstract + references|PDF
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The human PAX6 gene is mutated in two patients with aniridiapp328 - 332 Tim Jordan, Isabel Hanson, Dmitri Zaletayev, Shirley Hodgson, Jane Prosser, Anne Seawright, Nicholas Hastie
& Veronica van Heyningen doi:10.1038/ng0892-328 Abstract + references|PDF
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The human pseudoautosomal GM−CSF receptor subunit gene is autosomal in mousepp333 - 336 Christine M. Disteche, Camilynn I. Brannan, Alf Larsen, David A. Adler, Daniel F. Schorderet, David Gearing, Neal G. Copeland, Nancy A. Jenkins
& Linda S. Park doi:10.1038/ng0892-333 Abstract + references|PDF
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Kallmann syndrome due to a translocation resulting in an X/Y fusion genepp337 - 340 S. Guioli, B. Incerti, E. Zanaria, B. Bardoni, B. Franco, K. Taylor, A. Ballabio
& G. Camerino doi:10.1038/ng0892-337 Abstract + references|PDF
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Fragile X syndrome without CCG amplification has an FMR1 deletionpp341 - 344 A.K. Gedeon, E. Baker, H. Robinson, M.W. Partington, B. Gross, A. Manca, B. Korn, A. Poustka, S. Yu, G.R. Sutherland1
& J.C. Mulley doi:10.1038/ng0892-341 Abstract + references|PDF
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A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N−terminus of −amyloidpp345 - 347 Mike Mullan, Fiona Crawford, Karin Axelman, Henry Houlden, Lena Lilius, Bengt Winblad
& Lars Lannfelt doi:10.1038/ng0892-345 Abstract + references|PDF
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Expressed genes, Alu repeats and polymorphisms in cosmids sequenced from chromosome 4p16.3pp348 - 353 W.R. McCombie, A. Martin-Gallardo, J.D. Gocayne, M. FitzGerald, M. Dubnick, J.M. Kelley, L. Castilla, L.I. Liu, S. Wallace, S. Trapp, D. Tagle, W.L. Whaley, S. Cheng, J. Gusella, A.-M. Frischauf, A. Poustka, H. Lehrach, F. S. Collins, A. R. Kerlavage, C. Fields
& J.C. Venter doi:10.1038/ng0892-348 Abstract + references|PDF
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C1 inhibitor hinge region mutations produce dysfunction by different mechanismspp354 - 358 Alvin E. Davis III, Kulwant Aulak, Richard B. Parad, Hilary P. Stecklein, Eric Eldering, C. Erik Hack, Judit Kramer, Robert C. Strunk, John Bissler
& Fred S. Rosen doi:10.1038/ng0892-354 Abstract + references|PDF
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Molecular analysis of the muscle pathology associated with mitochondrial DNA deletionspp359 - 367 Carlos T. Moraes, Enzo Ricci, Vittoria Petruzzella, Sara Shanske, Salvatore DiMauro, Eric A. Schon
& Eduardo Bonilla doi:10.1038/ng0892-359 Abstract + references|PDF
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Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafnesspp368 - 371 J.M.W. van den Ouweland, H.H.P.J. Lemkes, W. Ruitenbeek, L.A. Sandkuijl, M.F. de Vijlder, P.A.A. Struyvenberg, J.J.P. van de Kamp
& J.A. Maassen doi:10.1038/ng0892-368 Abstract + references|PDF
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Adenovirus−mediated in vivo gene transfer and expression in normal rat liverpp372 - 378 H. A. Jaffe, C. Danel, G. Longenecker, M. Metzger, Y. Setoguchi, M. A. Rosenfeld, T. W. Gant, S. S. Thorgeirsson, L. D. Stratford-Perricaudet, M. Perricaudet, A. Pavirani, J.-P. Lecocq
& R. G. Crystal doi:10.1038/ng0892-372 Abstract + references|PDF
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Herpesvirus vector gene transfer and expression of −glucuronidase in the central nervous system of MRS VII micepp379 - 384 John H. Wolfe, Satish L. Deshmane
& Nigel W. Fraser doi:10.1038/ng0892-379 Abstract + references|PDF
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