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Your search keyword '"Reinecke, Robert"' showing total 3 results
Start Over Author "Reinecke, Robert" Journal nature genetics
3 results on '"Reinecke, Robert"'

1. Erratum: Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Author

Tarpey, Patrick, primary, Thomas, Shery, additional, Sarvananthan, Nagini, additional, Mallya, Uma, additional, Lisgo, Steven, additional, Talbot, Chris J, additional, Roberts, Eryl O, additional, Awan, Musarat, additional, Surendran, Mylvaganam, additional, McLean, Rebecca J, additional, Reinecke, Robert D, additional, Langmann, Andrea, additional, Lindner, Susanne, additional, Koch, Martina, additional, Jain, Sunila, additional, Woodruff, Geoffrey, additional, Gale, Richard P, additional, Degg, Chris, additional, Droutsas, Konstantinos, additional, Asproudis, Ioannis, additional, Zubcov, Alina A, additional, Pieh, Christina, additional, Veal, Colin D, additional, Machado, Rajiv D, additional, Backhouse, Oliver C, additional, Baumber, Laura, additional, Constantinescu, Cris S, additional, Brodsky, Michael C, additional, Hunter, David G, additional, Hertle, Richard W, additional, Read, Randy J, additional, Edkins, Sarah, additional, O'Meara, Sarah, additional, Parker, Adrian, additional, Stevens, Claire, additional, Teague, Jon, additional, Wooster, Richard, additional, Futreal, P Andrew, additional, Trembath, Richard C, additional, Stratton, Michael R, additional, Raymond, F Lucy, additional, and Gottlob, Irene, additional

Published
2011
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2. Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Author

Tarpey, Patrick, primary, Thomas, Shery, additional, Sarvananthan, Nagini, additional, Mallya, Uma, additional, Lisgo, Steven, additional, Talbot, Chris J, additional, Roberts, Eryl O, additional, Awan, Musarat, additional, Surendran, Mylvaganam, additional, McLean, Rebecca J, additional, Reinecke, Robert D, additional, Langmann, Andrea, additional, Lindner, Susanne, additional, Koch, Martina, additional, Jain, Sunila, additional, Woodruff, Geoffrey, additional, Gale, Richard P, additional, Bastawrous, Andrew, additional, Degg, Chris, additional, Droutsas, Konstantinos, additional, Asproudis, Ioannis, additional, Zubcov, Alina A, additional, Pieh, Christina, additional, Veal, Colin D, additional, Machado, Rajiv D, additional, Backhouse, Oliver C, additional, Baumber, Laura, additional, Constantinescu, Cris S, additional, Brodsky, Michael C, additional, Hunter, David G, additional, Hertle, Richard W, additional, Read, Randy J, additional, Edkins, Sarah, additional, O'Meara, Sarah, additional, Parker, Adrian, additional, Stevens, Claire, additional, Teague, Jon, additional, Wooster, Richard, additional, Futreal, P Andrew, additional, Trembath, Richard C, additional, Stratton, Michael R, additional, Raymond, F Lucy, additional, and Gottlob, Irene, additional

Published
2006
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3. Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.

Author

Tarpey, Patrick, Thomas, Shery, Sarvananthan, Nagini, Mallya, Uma, Lisgo, Steven, Talbot, Chris J, Roberts, Eryl O, Awan, Musarat, Surendran, Mylvaganam, McLean, Rebecca J, Reinecke, Robert D, Langmann, Andrea, Lindner, Susanne, Koch, Martina, Jain, Sunila, Woodruff, Geoffrey, Gale, Richard P, Degg, Chris, Droutsas, Konstantinos, and Asproudis, Ioannis

Subjects
AUTHORS
Abstract

A correction to the article "Mutations in FRMD7, a Newly Identified Member of the FERM Family, Cause X-Linked Idiopathic Congenital Nystagmus," that was published online October 1, 2006 issue and appeared in the November 2006 printed edition is presented.

Published
2011
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