Establishment of developmental gene silencing by ordered polycomb complex recruitment in early zebrafish embryos by Hickey, Graham Jm, Wike, Candice L, Nie, Xichen, Guo, Yixuan, Tan, Mengyao, Murphy, Patrick J, Cairns, Bradley R

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Spectrum of CHD7 Mutations in 110 Individuals with CHARGE Syndrome and Genotype-Phenotype Correlation by Lalani, Seema R., Safiullah, Arsalan M., Fernbach, Susan D., Harutyunyan, Karine G., Thaller, Christina, Peterson, Leif E., McPherson, John D., Gibbs, Richard A., White, Lisa D., Hefner, Margaret, Davenport, Sandra L.H., Graham, John M., Bacino, Carlos A., Glass, Nancy L., Towbin, Jeffrey A., Craigen, William J., Neish, Steven R., Lin, Angela E., Belmont, John W.

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Molar tooth sign of the midbrain-hindbrain junction: Occurrence in multiple distinct syndromes by Gleeson, Joseph G., Keeler, Lesley C., Parisi, Melissa A., Marsh, Sarah E., Chance, Phillip F., Glass, Ian A., Graham Jr, John M., Maria, Bernard L., Barkovich, A. James, Dobyns, William B.

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A Locus for Bilateral Perisylvian Polymicrogyria Maps to Xq28 by Villard, Laurent, Nguyen, Karine, Cardoso, Carlos, Martin, Christa Lese, Weiss, Ann M., Sifry-Platt, Mara, Grix, Arthur W., Graham, John M., Winter, Robin M., Leventer, Richard J., Dobyns, William B.

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Cerebro-Oculo-Facio-Skeletal Syndrome with a Nucleotide Excision–Repair Defect and a Mutated XPD Gene, with Prenatal Diagnosis in a Triplet Pregnancy by Graham, John M., Anyane-Yeboa, Kwame, Raams, Anja, Appeldoorn, Esther, Kleijer, Wim J., Garritsen, Victor H., Busch, David, Edersheim, Terri G., Jaspers, Nicolaas G.J.

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Down Syndrome Phenotypes: The Consequences of Chromosomal Imbalance by Korenberg, J. R., X.-N. Chen, Schipper, R., Sun, Z., Gonsky, R., Gerwehr, S., Carpenter, N., Daumer, C., Dignan, P., Disteche, C., Graham, J. M., Hudgins, L., McGillivray, B., Miyazaki, K., Ogasawara, N., Park, J. P., Pagon, R., Pueschel, S., Sack, G., Say, B., Schuffenhauer, S., Soukup, S., Yamanaka, T.

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Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephaly by Alcantara, Diana, Timms, Andrew E, Gripp, Karen, Baker, Laura, Park, Kaylee, Collins, Sarah, Cheng, Chi, Stewart, Fiona, Mehta, Sarju G, Saggar, Anand, Sztriha, László, Zombor, Melinda, Caluseriu, Oana, Mesterman, Ronit, Van Allen, Margot I, Jacquinet, Adeline, Ygberg, Sofia, Bernstein, Jonathan A, Wenger, Aaron M, Guturu, Harendra, Bejerano, Gill, Gomez-Ospina, Natalia, Lehman, Anna, Alfei, Enrico, Pantaleoni, Chiara, Conti, Valerio, Guerrini, Renzo, Moog, Ute, Graham, Jr, John M, Hevner, Robert, Dobyns, William B, O'Driscoll, Mark, Mirzaa, Ghayda M

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Ehlers-Danlos arthrochalasia type (VIIA-B) - expanding the phenotype: from prenatal life through adulthood by Klaassens, M, Reinstein, E, Hilhorst-Hofstee, Y, Schrander, JJP, Malfait, F, Staal, H, ten Have, LC, Blaauw, J, Roggeveen, HCJ, Krakow, D, De Paepe, A, van Steensel, MAM, Pals, G, Graham, JM, Schrander-Stumpel, CTRM

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The spectrum of mutations in UBE3A causing Angelman syndrome by PING FANG, LEV-LEHMAN, E, LANGLOIS, S, GRAHAM, J. M, BEUTEN, J, WILLEMS, P. J, LEDBETTER, D. H, BEAUDET, A. L, TSAI, T.-F, MATSUURA, T, BENTON, C. S, SUTCLIFFE, J. S, CHRISTIAN, S. L, KUBOTA, T, HALLEY, D. J, MEIJERS-HEIJBOER, H

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Syndromic Ear Anomalies and Renal Ultrasounds by Wang, Raymond Y, Earl, Dawn L, Ruder, Robert O, Graham Jr, John M

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Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia by Wiessner, Manuela, Maroofian, Reza, Ni, Meng-Yuan, Pedroni, Andrea, Müller, Juliane S, Stucka, Rolf, Beetz, Christian, Efthymiou, Stephanie, Santorelli, Filippo M, Alfares, Ahmed A, Zhu, Changlian, Uhrova Meszarosova, Anna, Alehabib, Elham, Bakhtiari, Somayeh, Janecke, Andreas R, Otero, Maria Gabriela, Chen, Jin Yun Helen, Peterson, James T, Strom, Tim M, De Jonghe, Peter, Deconinck, Tine, De Ridder, Willem, De Winter, Jonathan, Pasquariello, Rossella, Ricca, Ivana, Alfadhel, Majid, van de Warrenburg, Bart P, Portier, Ruben, Bergmann, Carsten, Ghasemi Firouzabadi, Saghar, Jin, Sheng Chih, Bilguvar, Kaya, Hamed, Sherifa, Abdelhameed, Mohammed, Haridy, Nourelhoda A, Maqbool, Shazia, Rahman, Fatima, Anwar, Najwa, Carmichael, Jenny, Pagnamenta, Alistair, Wood, Nick W, Tran Mau-Them, Frederic, Haack, Tobias, Di Rocco, Maja, Ceccherini, Isabella, Iacomino, Michele, Zara, Federico, Salpietro, Vincenzo, Scala, Marcello, Rusmini, Marta, Xu, Yiran, Wang, Yinghong, Suzuki, Yasuhiro, Koh, Kishin, Nan, Haitian, Ishiura, Hiroyuki, Tsuji, Shoji, Lambert, Laëtitia, Schmitt, Emmanuelle, Lacaze, Elodie, Küpper, Hanna, Dredge, David, Skraban, Cara, Goldstein, Amy, Willis, Mary J H, Grand, Katheryn, Graham, John M, Lewis, Richard A, Millan, Francisca, Duman, Özgür, Dündar, Nihal, Uyanik, Gökhan, Schöls, Ludger, Nürnberg, Peter, Nürnberg, Gudrun, Catala Bordes, Andrea, Seeman, Pavel, Kuchar, Martin, Darvish, Hossein, Rebelo, Adriana, Bouçanova, Filipa, Medard, Jean-Jacques, Chrast, Roman, Auer-Grumbach, Michaela, Alkuraya, Fowzan S, Shamseldin, Hanan, Al Tala, Saeed, Rezazadeh Varaghchi, Jamileh, Najafi, Maryam, Deschner, Selina, Gläser, Dieter, Hüttel, Wolfgang, Kruer, Michael C, Kamsteeg, Erik-Jan, Takiyama, Yoshihisa, Züchner, Stephan, Baets, Jonathan, Synofzik, Matthis, Schüle, Rebecca, Horvath, Rita

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Consequences of Not Interpreting Structure Coefficients in Published CFA Research: A Reminder by Graham, James M., Guthrie, Abbie C., Thompson, Bruce

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A new X-linked syndrome with agenesis of the corpus callosum, mental retardation, coloboma, micrognathia, and a mutation in the Alpha 4 gene at Xq13 by Graham Jr, John M., Wheeler, Patricia, Tackels-Horne, Darci, Lin, Angela E., Hall, Bryan D., May, Melanie, Short, Kieran M., Schwartz, Charles E., Cox, Timothy C.

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An epidemiological analysis of CHARGE syndrome: Preliminary results from a Canadian study by Issekutz, Karina A., Graham Jr, John M., Prasad, Chitra, Smith, Isabel M., Blake, Kim D.

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Management of deformational plagiocephaly: Repositioning versus orthotic therapy by Graham, John M., Gomez, Mayela, Halberg, Andy, Earl, Dawn L., Kreutzman, Jeannie T., Cui, Jinrui, Guo, Xiuqing

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Severe uncontrolled pain in buttock in a patient on naltrexone : A diagnostic challenge by GRAHAM, J. M, EVANS, B

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Phenotype-genotype correlations in patients with Marinesco-Sjögren syndrome by Ezgu, F., Krejci, P., Li, S., de Sousa, C., Graham Jr, J.M., Hansmann, I., He, W., Porpora, K., Wand, D., Wertelecki, W., Schneider, A., Wilcox, W.R.

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Impacts of large-scale atmospheric-ocean variability on Alaskan fire season severity by Duffy, P.A, Walsh, J.E, Graham, J.M, Mann, D.H, Rupp, T.S

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effects of arbuscular mycorrhizas on soil aggregation depend on the interaction between plant and fungal species by Piotrowski, J. S., Denich, T., Klironomos, J. N., Graham, J. M., Rillig, M. C.

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Cross-Modal Plasticity Underpins Language Recovery after Cochlear Implantation by Giraud, Anne-Lise, Price, Cathy J, Graham, John M, Truy, Eric, Frackowiak, Richard S.J

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