BRCA1 protein products: Antibody specificity...pp264 - 265 Cindy A. Wilson, Marc N. Payton, Susan K. Pekar, Ke Zhang, Robert E. Pacifici, Jean L. Gudas, Sushil Thukral, Frank J. Calzone, David M. Reese
& Dennis I. Slamon doi:10.1038/ng0796-264 References|PDF
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...Functional motifs...pp266 - 268 Eugene V. Koonin, Stephen F. Altschul
& Peer Bork doi:10.1038/ng0796-266 References|PDF
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...and secreted tumour suppressorspp268 - 269 Allan Bradley
& Shyam K. Sharan doi:10.1038/ng0796-268b References|PDF
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Reply to "...and secreted tumour suppressors"pp269 - 272 Roy A. Jensen, Marilyn E. Thompson, Thomas L. Jetton, Riet van der Meer, Bassam Helou, Carlos L. Arteaga, David L. Page, Jeffrey T. Holt, Steven R. Tronick, Allen M. Gown, Marilyn Skelly, Beth Ostermeyer, David Schieltz, Csilla I. Szabo
& Mary-Claire King doi:10.1038/ng0796-269 References|PDF
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LIM−kinase deleted in Williams syndromepp272 - 273 Mayada Tassabehji, Kay Metcalfe, William D. Fergusson, Martin J.A. Carette, Jonathan K. Dore, Dian Donnai, Andrew P. Read, C. Pröschel, N.J. Gutowski, Xin Mao
& Denise Sheer doi:10.1038/ng0796-272 References|PDF
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Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox genepp275 - 283 Qi Zhao, Richard R. Behringer
& Benoit de Crombrugghe doi:10.1038/ng0796-275 Abstract + references|PDF
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The molecular basis of hypodactyly (Hd): a deletion in Hoxa13 leads to arrest of digital arch formationpp284 - 289 Douglas P. Mortlock, Laura C. Post
& Jeffrey W. Innis doi:10.1038/ng0796-284 Abstract + references|PDF
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Spontaneous in vivo reversion to normal of an inherited mutation in a patient with adenosine deaminase deficiencypp290 - 295 Rochelle Hirschhorn, Diana Ruixi Yang, Jennifer M. Puck, Maryann L. Huie, Chuan-Kui Jiang
& Lawrence E. Kurlandsky doi:10.1038/ng0796-290 Abstract + references|PDF
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A single mouse gene encodes the mitochondrial transcription factor A and a testis−specific nuclear HMG-box proteinpp296 - 302 Nils-Göran Larsson, J. David Garman, Anders Oldfors, Gregory S. Barsh
& David A. Clayton doi:10.1038/ng0796-296 Abstract + references|PDF
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Identification of the murine beige gene by YAC complementation and positional cloningpp303 - 308 Charles M. Perou, Karen J. Moore, Deborah L. Nagle, Donald J. Misumi, Elizabeth A. Woolf, Sonja H. McGrail, Lisa Holmgren, Thomas H. Brody, Barry J. Dussault Jr., Cheryl A. Monroe, Geoffrey M. Duyk, Robert J. Pryor, Liangtao Li, Monica J. Justice
& Jerry Kaplan doi:10.1038/ng0796-303 Abstract + references|PDF
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Signalling by the W/Kit receptor tyrosine kinase is negatively regulated in vivo by the protein tyrosine phosphatase Shp1pp309 - 315 Robert F. Paulson, Shirly Vesely, Katharine A. Siminovitch
& Alan Bernstein doi:10.1038/ng0796-309 Abstract + references|PDF
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Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in micepp316 - 324 Gert Jansen, Patricia J.T.A. Groenen, Dietmar Bächner, Paul H.K. Jap, Marga Coerwinkel, Frank Oerlemans, Walther van den Broek, Bärbel Gohlsch, Dirk Pette, Jaap J. Plomp, Peter C. Molenaar, Marcel G.J. Nederhoff, Cees J.A. van Echteld, Marleen Dekker, Anton Berns, Horst Hameister
& Bé Wieringa doi:10.1038/ng0796-316 Abstract + references|PDF
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Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathypp325 - 335 Sita Reddy, Daniel B. J. Smith, Mark M. Rich, John M. Leferovich, Patricia Reilly, Brigid M. Davis, Khoa Tran, Helen Rayburn, Roderick Bronson, Didier Cros, Rita J. Balice-Gordon
& David Housman doi:10.1038/ng0796-325 Abstract + references|PDF
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Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing overpp336 - 342 Sean M. Baker, Annemieke W. Plug, Tomas A. Prolla, C. Eric Bronner, Allie C. Harris, Xiang Yao, Donna-Marie Christie, Craig Monell, Norm Arnheim, Allan Bradley, Terry Ashley
& R. Michael Liskay doi:10.1038/ng0796-336 Abstract + references|PDF
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Evaluation of candidate tumour suppressor genes on chromosome 18 in colorectal cancerspp343 - 346 Sam Thiagalingam, Christoph Lengauer, Frederick S. Leach, Mieke Schutte, Stephan A. Hahn, Joan Overhauser, James K.V. Willson, Sanford Markowitz, Stanley R. Hamilton, Scott E. Kern, Kenneth W. Kinzler
& Bert Vogelstein doi:10.1038/ng0796-343 Abstract + references|PDF
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Mad-related genes in the humanpp347 - 349 Gregory J. Riggins, Sam Thiagalingam, Ester Rozenblum, Craig L. Weinstein, Scott E. Kern, Stanley R. Hamilton, James K.V. Willson, Sanford D. Markowitz, Kenneth W. Kinzler
& Bert Vogelstein doi:10.1038/ng0796-347 Abstract + references|PDF
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Accelerated telomere shortening in ataxia telangiectasiapp350 - 353 Judith A. Metcalfe, Julian Parkhill, Louise Campbell, Michael Stacey, Paul Biggs, Philip J. Byrd
& A. Malcolm R. Taylor doi:10.1038/ng0796-350 Abstract + references|PDF
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Thyroid hormone receptor is essential for development of auditory functionpp354 - 357 Douglas Forrest, Lawrence C. Erway, Lily Ng, Richard Altschuler
& Tom Curran doi:10.1038/ng0796-354 Abstract + references|PDF
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Missense mutation in the gene encoding the subunit of rod transducin in the Nougaret form of congenital stationary night blindnesspp358 - 360 Thaddeus P. Dryja, Lauri B. Hahn, Thierry Reboul
& Bernard Arnaud doi:10.1038/ng0796-358 Abstract + references|PDF
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A translocation interrupts the COL5A1 gene in a patient with Ehlers−Danlos syndrome and hypomelanosis of Itopp361 - 365 Helga V. Toriello, Thomas W. Glover, Kazuhiko Takahara, Peter H. Byers, Diane E. Miller, James V. Higgins
& Daniel S. Greenspan doi:10.1038/ng0796-361 Abstract + references|PDF
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Epithelial detachment due to absence of hemidesmosomes in integrin 4 null micepp366 - 369 Ronald van der Neut, Paul Krimpenfort, Jero Calafat, Carien M. Niessen
& Arnoud Sonnenberg doi:10.1038/ng0796-366 Abstract + references|PDF
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Absence of integrin 6 leads to epidermolysis bullosa and neonatal death in micepp370 - 373 Elisabeth Georges-Labouesse, Nadia Messaddeq, Ghassan Yehia, Laurence Cadalbert, Andrée Dierich
& Marianne Le Meur doi:10.1038/ng0796-370 Abstract + references|PDF
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Erratum: Effective treatment of familial hypercholesterolaemia in the mouse model using adenovirus-mediated transfer of the VLDL receptor genep374 doi:10.1038/ng0796-374a PDF
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Erratum: Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer familiesp374 doi:10.1038/ng0796-374b PDF
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is essential for development of auditory function
subunit of rod transducin in the Nougaret form of congenital stationary night blindness
4 null mice
