Homozygous 15q13.3 microdeletion in a child with hypotonia and impaired vision: A new report and review of the literature von Simon, Julie, Stoll, Katie, Fick, Roger, Mott, Jared, Lawson‐Yuen, Amy

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Recurrent duplications of 17q12 associated with variable phenotypes von Mitchell, Elyse, Douglas, Andrew, Kjaegaard, Susanne, Callewaert, Bert, Vanlander, Arnaud, Janssens, Sandra, Yuen, Amy Lawson, Skinner, Cindy, Failla, Pinella, Alberti, Antonino, Avola, Emanuela, Fichera, Marco, Kibaek, Maria, Digilio, Maria C., Hannibal, Mark C., den Hollander, Nicolette S., Bizzarri, Veronica, Renieri, Alessandra, Mencarelli, Maria Antonietta, Fitzgerald, Tomas, Piazzolla, Serena, van Oudenhove, Elke, Romano, Corrado, Schwartz, Charles, Eichler, Evan E., Slavotinek, Anne, Escobar, Luis, Rajan, Diana, Crolla, John, Carter, Nigel, Hodge, Jennelle C., Mefford, Heather C.

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Atypical cases of Angelman syndrome von Lawson‐Yuen, Amy, Wu, Bai‐Lin, Lip, Va, Sahoo, Trilochan, Kimonis, Virginia

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Familial deletion within NLGN4 associated with autism and Tourette syndrome von Lawson-Yuen, Amy, Saldivar, Juan-Sebastian, Sommer, Steve, Picker, Jonathan

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The use of betaine in the treatment of elevated homocysteine von Lawson-Yuen, Amy, Levy, Harvey L.

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Ube3a mRNA and protein expression are not decreased in Mecp2 mutant mice von Lawson-Yuen, Amy, Liu, Daniel, Han, Liqun, Jiang, Zhichun I., Tsai, Guochuan E., Basu, Alo C., Picker, Jonathan, Feng, Jiamin, Coyle, Joseph T.

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Ube3a mRNA and protein expression are not decreased in Mecp2R168X mutant mice von LAWSON-YUEN, Amy, LIU, Daniel, LIQUN HAN, JIANG, Zhichun I, TSAI, Guochuan E, BASU, Alo C, PICKER, Jonathan, JIAMIN FENG, COYLE, Joseph T

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Ube3a mRNA and protein expression are not decreased in Mecp2 R168X mutant mice von Lawson-Yuen, Amy, Liu, Daniel, Han, Liqun, Jiang, Zhichun I, Tsai, Guochuan E, Basu, Alo C, Picker, Jonathan, Feng, Jiamin, Coyle, Joseph T

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Homozygous 15q13.3 microdeletion in a child with hypotonia and impaired vision: A new report and review of the literature von Simon, Julie, Stoll, Katie, Fick, Roger, Mott, Jared, Lawson-Yuen, Amy

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Atypical cases of Angelman syndrome von Lawson-Yuen, Amy, Wu, Bai-Lin, Lip, Va, Sahoo, Trilochan, Kimonis, Virginia

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DNM1 encephalopathy: A new disease of vesicle fission von von Spiczak, Sarah, Helbig, Katherine L, Shinde, Deepali N, Huether, Robert, Pendziwiat, Manuela, Lourenço, Charles, Nunes, Mark E, Sarco, Dean P, Kaplan, Richard A, Dlugos, Dennis J, Kirsch, Heidi, Slavotinek, Anne, Cilio, Maria R, Cervenka, Mackenzie C, Cohen, Julie S, McClellan, Rebecca, Fatemi, Ali, Yuen, Amy, Sagawa, Yoshimi, Littlejohn, Rebecca, McLean, Scott D, Hernandez-Hernandez, Laura, Maher, Bridget, Møller, Rikke S, Palmer, Elizabeth, Lawson, John A, Campbell, Colleen A, Joshi, Charuta N, Kolbe, Diana L, Hollingsworth, Georgie, Neubauer, Bernd A, Muhle, Hiltrud, Stephani, Ulrich, Scheffer, Ingrid E, Pena, Sérgio D.J, Sisodiya, Sanjay M, Helbig, Ingo

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