Sökresultat - Louise Christie
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Expanding the molecular basis and phenotypic spectrum of X-linked Joubert syndrome associated with OFD1 mutations av Michael Field, Ingrid E. Scheffer, Deepak Gill, Meredith Wilson, Louise Christie, Marie Shaw, Alison Gardner, Georgie C. Glubb, Lynne Hobson, Mark Corbett, Kathryn Friend, Saffron A.G. Willis‐Owen, Jozef Gécz
Publicerad 2012Artigo -
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Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation av Reinhard Ullmann, Gillian Turner, Maria Kirchhoff, Wei Chen, Bruce J. Tonge, Carla Rosenberg, Michael Field, Angela Maria Vianna‐Morgante, Louise Christie, Ana Cristina Victorino Krepischi, Lynn Banna, Avril V. Brereton, Alyssa C. Hill, Anne‐Marie Bisgaard, Ines Müller, Claus Hultschig, Fikret Erdogan, Georg Wieczorek, Hans‐Hilger Ropers
Publicerad 2007Artigo -
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X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes av Hao Hu, Stefan A. Haas, Jamel Chelly, Hilde Van Esch, Martine Raynaud, Arjan P.M. de Brouwer, Stefanie Weinert, Guy Froyen, Suzanna G.M. Frints, Frédéric Laumonnier, Tomasz Żemojtel, Michael I. Love, Hugues Richard, A-K Emde, Melanie Bienek, Corinna Jensen, M Hambrock, Utz Fischer, Claudia Langnick, Mirjam Feldkamp, W.M. Wissink-Lindhout, Nicolas Lebrun, L. Castelnau, J. Rucci, Rodrick Montjean, Olivier Dorseuil, Pierre Billuart, Till Stuhlmann, M Shaw, Mark Corbett, Alison Gardner, Saffron A.G. Willis‐Owen, Chuan Tan, Kathryn Friend, Stefanie Belet, Kees E. P. van Roozendaal, M Jimenez-Pocquet, M.‐P. Moizard, Nathalie Ronce, Ren Sun, Sean O’Keeffe, R Chenna, Alena van Bömmel, Jonathan Göke, Anna Hackett, Michael Field, Louise Christie, Jackie Boyle, Eric Haan, John W. Nelson, Gillian Turner, Gareth Baynam, Gabriele Gillessen‐Kaesbach, Ulrich Müller, Daniela Steinberger, Bartłomiej Budny, Magdalena Badura‐Stronka, Anna Latos‐Bieleńska, Lilian Bomme Ousager, Peter Wieacker, Germán Rodríguez Criado, M.-L. Bondeson, Göran Annerén, Andreas Dufke, Monika Cohen, Lionel Van Maldergem, C. Vincent‐Delorme, Bernard Échenne, Brigitte Simon‐Bouy, Tjitske Kleefstra, Marjolein H. Willemsen, J-P. Fryns, Koenraad Devriendt, Reinhard Ullmann, Martin Vingron, Klaus Wrogemann, Thomas F. Wienker, Andreas Tzschach, Hans van Bokhoven, Jozef Gécz, Thomas J. Jentsch, W. Chen, H‐H Ropers, Vera M. Kalscheuer
Publicerad 2015Artigo
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Relaterade ämnen
Biology
Gene
Genetics
Chromosome
Comparative genomic hybridization
Exome sequencing
Gene duplication
Psychology
Autism
Chromosomal translocation
Chromosome 21
Computational biology
Copy-number variation
DNA sequencing
Developmental disorder
Epilepsy
Exome
Exon
Fluorescence in situ hybridization
Gene family
Genetic heterogeneity
Genome
Intellectual disability
Joubert syndrome
Karyotype
Massive parallel sequencing
Mutation
Neuroscience
Phenotype
Polymicrogyria