Schizophrenia susceptibility and chromosome 6p24−22pp233 - 234 Bryan J. Mowry, Derek J. Nancarrow, David P. Lennon, Lodewijk A. Sandkuijl, Raymond R. Crowe, Jeremy M. Silverman, Richard C. Mohs, Larry J. Siever, Jean Endicott, Lawrence Sharpe, Marilyn K. Walters, Nicholas K. Hayward
& Douglas F. Levinson doi:10.1038/ng1195-233 References|PDF
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Schizophrenia susceptibility and chromosome 6p24−22pp234 - 235 Hugh Gurling, Gursharan Kalsi, Andrew Hui-Sui Chen, Melanie Green, Robert Butler, Tim Read, Patrice Murphy, David Curtis, Tonmoy Sharma, Hannes Petursson
& Jon Brynjolfsson doi:10.1038/ng1195-234 References|PDF
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Schizophrenia susceptibility and chromosome 6p24−22pp235 - 236 Stylianos E Antonarakis, Jean-Louis Blouin, Ann E. Pulver, Paula Wolyniec, Virginia K. Lasseter, Gerald Nestadt, Laura Kasch, Robert Babb, Haig H. Kazazian, Beth Dombroski, Michelle Kimberland, Jurg Ott, David Housman, Maria Karayiorgou
& Charles J. MacLean doi:10.1038/ng1195-235 References|PDF
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A chromatin model of IGF2/H19 imprintingpp237 - 238 Subhasis Banerjee
& Alan Smallwood doi:10.1038/ng1195-237 References|PDF
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Breast cancer information on the webpp238 - 239 Stephen Friend, Anne-Lise Borresen, Larry Brody, Graham Casey, Peter Devilee, Simon Gayther, David Goldgar, Pat Murphy, Barbara L. Weber
& Roger Wiseman doi:10.1038/ng1195-238 PDF
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Genetic dissection of complex traits: guidelines for interpreting and reporting linkage resultspp241 - 247 Eric Lander
& Leonid Kruglyak doi:10.1038/ng1195-241 Abstract + references|PDF
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Linkage between sexual orientation and chromosome Xq28 in males but not in femalespp248 - 256 Stella Hu, Angela M. L. Pattatucci, Chavis Patterson, Lin Li, David W. Fulker, Stacey S. Cherny, Leonid Kruglyak
& Dean H. Hamer doi:10.1038/ng1195-248 Abstract + references|PDF
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−sarcoglycan: characterization and role in limb−girdle muscular dystrophy linked to 4q12pp257 - 265 Leland E. Lim, Franck Duclos, Odile Broux, Nathalie Bourg, Yoshihide Sunada, Valérie Allamand, Jon Meyer, Isabelle Richard, Carolyn Moomaw, Clive Slaughter, Fernando M.S. Tomé, Michel Fardeau, Charles E. Jackson, Jacques S. Beckmann
& Kevin P. Campbell doi:10.1038/ng1195-257 Abstract + references|PDF
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−sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complexpp266 - 273 Carsten G. Bönnemann, Raju Modi, Satoru Noguchi, Yuji Mizuno, Mikiharu Yoshida, Emanuela Gussoni, Elizabeth M. McNally, David J. Duggan, Corrado Angelini, Eric P. Hoffman, Eijiro Ozawa
& Louis M. Kunkel doi:10.1038/ng1195-266 Abstract + references|PDF
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Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient micepp274 - 280 Katrin Adlkofer, Rudolf Martini, Adriano Aguzzi, Jürgen Zielasek, Klaus V. Toyka
& Ueli Suter doi:10.1038/ng1195-274 Abstract + references|PDF
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Protein zero (P0)−deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathiespp281 - 286 Rudolf Martini, Jürgen Zielasek, Klaus V. Toyka, K. Peter Giese
& Melitta Schachner doi:10.1038/ng1195-281 Abstract + references|PDF
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A potential vulnerability locus for schizophrenia on chromosome 6p24−22: evidence for genetic heterogeneitypp287 - 293 Richard E. Straub, Charles J. MacLean, F. Anthony O'Neill, John Burke, Bernadette Murphy, Fiona Duke, Rosemarie Shinkwin, Bradley T. Webb, Jie Zhang, Dermot Walsh
& Kenneth S. Kendler doi:10.1038/ng1195-287 Abstract + references|PDF
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Targeted mutation in the Fas gene causes hyperplasia in peripheral lymphoid organs and liverpp294 - 300 Masashi Adachi, Sachiko Suematsu, Toru Kondo, Jun Ogasawara, Takashi Tanaka, Nobuaki Yoshida
& Shigekazu Nagata doi:10.1038/ng1195-294 Abstract + references|PDF
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Evolution of the cryptic FMR1 CGG repeatpp301 - 308 Evan E. Eichler, Catherine B. Kunst, Kellie A. Lugenbeel, Oliver A. Ryder, Daniel Davison, Stephen T. Warren
& David L. Nelson doi:10.1038/ng1195-301 Abstract + references|PDF
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Developmental expression pattern screen for genes predicted in the C. elegans genome sequencing projectpp309 - 313 Andrew S. Lynch, David Briggs
& Ian A. Hope doi:10.1038/ng1195-309 Abstract + references|PDF
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Expression patterns of predicted genes from the C. elegans genome sequence visualized by FISH in whole organismspp314 - 320 Philip S. Birchall, Rita M. Fishpool
& Donna G. Albertson doi:10.1038/ng1195-314 Abstract + references|PDF
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An international two−stage genome−wide search for schizophrenia susceptibility genespp321 - 324 H.W. Moises, L. Yang, H. Kristbjarnarson, C. Wiese, W. Byerley, F. Macciardi, V. Arolt, D. Blackwood, X. Liu, B. Sjögren, H.N. Aschauer, H.-G. Hwu, K. Jang, W.J. Livesley, J.L. Kennedy, T. Zoega, O. Ivarsson, M.-T. Bui, M.-H. Yu, B. Havsteen, D. Commenges, J. Weissenbach, E. Schwinger, I.I. Gottesman, A.J. Pakstis, L. Wetterberg, K.K. Kidd
& T. Helgason doi:10.1038/ng1195-321 Abstract + references|PDF
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Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib−pair linkage analysispp325 - 327 Sibylle G. Schwab, Margot Albus, Joachim Hallmayer, Sabine Hönig, Margitta Borrmann, Dirk Lichtermann, Richard P. Ebstein, Manfred Ackenheil, Bernard Lerer, Neil Risch, Wolfgang Maier
& Dieter B. Wildenauer doi:10.1038/ng1195-325 Abstract + references|PDF
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Variants of the melanocyte−stimulating hormone receptor gene are associated with red hair and fair skin in humanspp328 - 330 Paloma Valverde, Eugene Healy, Ian Jackson, Jonathan L. Rees
& Anthony J. Thody doi:10.1038/ng1195-328 Abstract + references|PDF
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Contribution of the FMR1 gene mutation to human intellectual dysfunctionpp331 - 334 Allan L. Reiss, Lisa S. Freund, Thomas L. Baumgardner, Michael T. Abrams
& Martha B. Denckla doi:10.1038/ng1195-331 Abstract + references|PDF
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A frame−shift deletion in the survival motor neuron gene in Spanish spinal muscular atrophy patientspp335 - 337 Elena Bussaglia, Olivier Clermont, Eduardo Tizzano, Suzie Lefebvre, Lydie Bürglen, Corinne Cruaud, Jon Andoni Urtizberea, Jaume Colomer, Arnold Munnich, Montserrat Baiget
& Judith Melki doi:10.1038/ng1195-335 Abstract + references|PDF
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Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3pp338 - 340 Jan C. Pronk, Rachel A. Gibson, Anna Savoia, Mario Wijker, Neil V. Morgan, Salvatore Melchionda, Deborah Ford, Samia Temtamy, Juan J. Ortega, Stander Jansen, Charmaine Havenga, Richard J. Cohn, Thomy J. de Ravel, Irene Roberts, Andries Westerveld, Douglas F. Easton, Hans Joenje, Christopher G. Mathew
& Fré Arwert doi:10.1038/ng1195-338 Abstract + references|PDF
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Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3ppp341 - 343 Michael Whitney, Matt Thayer, Carol Reifsteck, Susan Olson, Leslie Smith, Petra M. Jakobs, Robin Leach, Susan Naylor, Hans Joenje
& Markus Grompe doi:10.1038/ng1195-341 Abstract + references|PDF
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Deficiency of the 3 subunit of the type A −aminobutyric acid receptor causes cleft palate in micepp344 - 346 Cymbeline T. Culiat, Lisa J. Stubbs, Richard P. Woychik, Liane B. Russell, Dabney K. Johnson
& Eugene M. Rinchik doi:10.1038/ng1195-344 Abstract + references|PDF
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Widespread expression of the testis−determining gene SRY in a marsupialpp347 - 349 Jenny L. Harry, Peter Koopman, Francine E. Brennan, Jennifer A. Marshall Graves
& Marilyn B. Renfree doi:10.1038/ng1195-347 Abstract + references|PDF
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−sarcoglycan: characterization and role in limb−girdle muscular dystrophy linked to 4q12
−aminobutyric acid receptor causes cleft palate in mice
