P195: Investigating the contribution of an intronic expansion repeat in FGF14 as a genetic cause of late-onset ataxia von Cuillerier, Alexanne, Mackay, Layla, Wall, Erika, Del Gobbo, Giulia, Seldenthuis, Luke, Mears, Wendy, White-Brown, Alexandre, Larrigan, Laura, Dyment, David, Boycott, Kym

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Online Library Accessibility Support: A Case Study within the Open University Library von Mears, Wendy, Clough, Helen

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ABHD16A deficiency causes a complicated form of hereditary spastic paraplegia associated with intellectual disability and cerebral anomalies von Lemire, Gabrielle, Ito, Yoko A., Marshall, Aren E., Chrestian, Nicolas, Stanley, Valentina, Brady, Lauren, Tarnopolsky, Mark, Curry, Cynthia J., Hartley, Taila, Mears, Wendy, Derksen, Alexa, Rioux, Nadie, Laflamme, Nataly, Hutchison, Harrol T., Pais, Lynn S., Zaki, Maha S., Sultan, Tipu, Dane, Adrie D., Gleeson, Joseph G., Vaz, Frédéric M., Kernohan, Kristin D., Bernard, Geneviève, Boycott, Kym M.

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Molecular characterization of 13 patients with PIK3CA‐related overgrowth spectrum using a targeted deep sequencing approach von Kock, Leanne, Cuillerier, Alexanne, Gillespie, Meredith, Couse, Madeline, Hartley, Taila, Mears, Wendy, Bernier, Francois P., Chudley, Albert E., Frosk, Patrick, Nikkel, Sarah M., Innes, A. Micheil, Lauzon, Julie, Thomas, Maryann, Guerin, Andrea, Armour, Christine M., Weksberg, Rosanna, Scott, James N., Watkins, Debra, Harvey, Shirley, Cytrynbaum, Cheryl, Kernohan, Kristin D., Boycott, Kym M.

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Diagnostic clarity of exome sequencing following negative comprehensive panel testing in the neonatal intensive care unit von Kernohan, Kristin D., Hartley, Taila, Naumenko, Sergey, Armour, Christine M., Graham, Gail E., Nikkel, Sarah M., Lines, Matthew, Geraghty, Michael T., Richer, Julie, Mears, Wendy, Boycott, Kym M., Dyment, David A.

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Yunis-Varón syndrome caused by biallelic VAC14 mutations von Lines, Matthew A, Ito, Yoko, Kernohan, Kristin D, Mears, Wendy, Hurteau-Miller, Julie, Venkateswaran, Sunita, Ward, Leanne, Khatchadourian, Karine, McClintock, Jeff, Bhola, Priya, Campeau, Philippe M, Boycott, Kym M, Michaud, Jean, van Kuilenburg, André Bp, Ferdinandusse, Sacha, Dyment, David A

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Expanding the Phenotypic Spectrum of GPI Anchoring Deficiency Due to Biallelic Variants in GPAA1 von Castle, Alison M. R., Salian, Smrithi, Bassan, Haim, Sofrin-Drucker, Efrat, Cusmai, Raffaella, Herman, Kristin C., Heron, Delphine, Keren, Boris, Johnstone, Devon L., Mears, Wendy, Morlot, Susanne, Nguyen, Thi Tuyet Mai, Rock, Rachel, Stolerman, Elliot, Russo, Julia, Burns, William Boyce, Jones, Julie R., Serpieri, Valentina, Wallaschek, Hannah, Zanni, Ginevra, Dyment, David A., Campeau, Philippe M.

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The RGG box motif of the herpes simplex virus ICP27 protein mediates an RNA-binding activity and determines in vivo methylation von Mears, W E, Rice, S A

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The Herpes Simplex Virus Immediate-Early Protein ICP27 Shuttles between Nucleus and Cytoplasm von Mears, Wendy E., Rice, Stephen A.

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Getting the message across: targeting distance learners using e-messaging von Reedy, Katharine, Mears, Wendy

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Identification of nuclear and nucleolar localization signals in the herpes simplex virus regulatory protein ICP27 von Mears, W E, Lam, V, Rice, S A

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Online library accessibility support: a case study within the Open University Library von Mears, Wendy, Clough, Helen

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BOOK REVIEWS von Bates, Tony, Mears, Wendy, Reedy, Katharine, Rumble, Greville

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BOOK REVIEWS von Bates, Tony, Mears, Wendy, Reedy, Katharine, Rumble, Greville

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Clinical Report—Head Lice von FRANKOWSKI, Barbara L, BOCCHINI, Joseph A

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Head lice von Frankowski, Barbara L, Bocchini, Jr, Joseph A

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