Plant Secondary Metabolites with an Overview of Populus von Movahedi, Ali, Almasi Zadeh Yaghuti, Amir, Wei, Hui, Rutland, Paul, Sun, Weibo, Mousavi, Mohaddeseh, Li, Dawei, Qiang, Zhuge

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Screening of interleukin 17F gene polymorphisms and eight subgingival pathogens in chronic periodontitis in Libyan patients von Alsherif, Eshraq, Alhudiri, Inas, ElJilani, Mouna, Ramadan, Ahmad, Rutland, Paul, Elzagheid, Adam, Enattah, Nabil

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Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome von Reardon, William, Winter, Robin M, Rutland, Paul, Pulleyn, Louise J, Jones, Barry M, Malcolm, Sue

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A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome von Muenke, Maximilian, Schell, Ute, Hehr, Andreas, Robin, Nathaniel H, Losken, H. Wolfgang, Schinzel, Albert, Pulleyn, Louise J, Rutland, Paul, Reardon, William, Malcolm, Sue, Winter, Robin M

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Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes von Rutland, Paul, Pulleyn, Louise J, Reardon, William, Baraitser, Michael, Hayward, Richard, Jones, Barry, Malcolm, Sue, Winter, Robin M, Oldridge, Michael, Slaney, Sarah F, Poole, Michael D, Wilkie, Andrew O.M

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Frameshift mutation in GJA12 leading to nystagmus, spastic ataxia and CNS dys-/demyelination von WOLF, Nicole I, CUNDALL, Maria, WOODWARD, Karen J, RUTLAND, Paul, ROSSER, Elisabeth, SURTEES, Robert, BENTON, Sarah, CHONG, Wui K, MALCOLM, Sue, EBINGER, Friedrich, BITNER-GLINDZICZ, Maria

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Genomic Insights into Cardiomyopathies: A Comparative Cross-Species Review von Simpson, Siobhan, Rutland, Paul, Rutland, Catrin Sian

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First report of Mycobacterium bovis DNA in human remains from the Iron Age von Taylor, G. Michael, Murphy, Eileen, Hopkins, Richard, Rutland, Paul, Chistov, Yuri

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Anatomy, histology, development and functions of Ossa cordis: A review von Best, Adam, Egerbacher, Monika, Swaine, Sophia, Pérez, William, Alibhai, Aziza, Rutland, Paul, Kubale, Valentina, El‐Gendy, Samir A. A., Alsafy, Mohamed A. M., Baiker, Kerstin, Sturrock, Craig J., Rutland, Catrin Sian

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Mitochondrial m.1584A 12S m62A rRNA methylation in families with m.1555A>G associated hearing loss von O'Sullivan, Mary, Rutland, Paul, Lucas, Deirdre, Ashton, Emma, Hendricks, Sebastian, Rahman, Shamima, Bitner-Glindzicz, Maria

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Mitochondrial m.1584A 12S m super(6) sub(2)A rRNA methylation in families with m.1555A>G associated hearing loss von O'Sullivan, Mary, Rutland, Paul, Lucas, Deirdre, Ashton, Emma, Hendricks, Sebastian, Rahman, Shamima, Bitner-Glindzicz, Maria

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FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy von Fassone, Elisa, Duncan, Andrew J, Taanman, Jan-Willem, Pagnamenta, Alistair T, Sadowski, Michael I, Holand, Tatjana, Qasim, Waseem, Rutland, Paul, Calvo, Sarah E, Mootha, Vamsi K, Bitner-Glindzicz, Maria, Rahman, Shamima

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Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein von Scambler, Peter J, McGregor, Lesley, Makela, Ville, Darling, Susan M, Vrontou, Sofia, Chalepakis, Georges, Roberts, Catherine, Smart, Nicola, Rutland, Paul, Prescott, Natalie, Hopkins, Jason, Bentley, Elizabeth, Shaw, Alison, Roberts, Emma, Mueller, Robert, Jadeja, Shalini, Philip, Nicole, Nelson, John, Francannet, Christine, Perez-Aytes, Antonio, Megarbane, Andre, Kerr, Bronwyn, Wainwright, Brandon, Woolf, Adrian S, Winter, Robin M

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A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene von Bitner-Glindzicz, Maria, Glaser, Benjamin, Lindley, Keith J, Rutland, Paul, Blaydon, Diana, Smith, Virpi V, Milla, Peter J, Hussain, Khalid, Furth-Lavi, Judith, Cosgrove, Karen E, Shepherd, Ruth M, Barnes, Philippa D, O'Brien, Rachel E, Farndon, Peter A, Sowden, Jane, Liu, Xue-Zhong, Scanlan, Matthew J, Malcolm, Sue, Dunne, Mark J, Aynsley-Green, Albert

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Mycobacterium leprae genotype amplified from an archaeological case of lepromatous leprosy in Central Asia von Taylor, G. Michael, Blau, Soren, Mays, Simon, Monot, Marc, Lee, Oona Y.-C., Minnikin, David E., Besra, Gurdyal S., Cole, Stewart T., Rutland, Paul

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FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy von Fassone, Elisa, Duncan, Andrew J., Taanman, Jan-Willem, Pagnamenta, Alistair T., Sadowski, Michael I., Holand, Tatjana, Qasim, Waseem, Rutland, Paul, Calvo, Sarah E., Mootha, Vamsi K., Bitner-Glindzicz, Maria, Rahman, Shamima

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Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome von Wilkie, Andrew O.M, Slaney, Sarah F, Oldridge, Michael, Poole, Michael D, Ashworth, Geraldine J, Hockley, Anthony D, Hayward, Richard D, David, David J, Pulleyn, Louise J, Rutland, Paul, Malcolm, Susan, Winter, Robin M, Reardon, William

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A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes von Idrees, Faisal, Bloch-Zupan, Agnes, Free, Samantha L., Vaideanu, Daniela, Thompson, Pamela J., Ashley, Paul, Brice, Glen, Rutland, Paul, Bitner-Glindzicz, Maria, Khaw, Peng T., Fraser, Scott, Sisodiya, Sanjay M., Sowden, Jane C.

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FLOTATION TOY von RUTLAND, Paul

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Flotation Toy von Paul Rutland

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