Holoprosencephaly due to mutations in ZIC2 , a homologue of Drosophila odd-paired von Brown, Stephen A, Warburton, Dorothy, Brown, Lucia Y, Yu, Chih-yu, Roeder, Elizabeth R, Stengel-Rutkowski, Sabine, Hennekam, Raoul C.M, Muenke, Maximilian

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Brain Abnormalities in Patients with Germline Variants in H3F3 : Novel Imaging Findings and Neurologic Symptoms Beyond Somatic Variants and Brain Tumors von Alves, C A P F, Sherbini, O, D'Arco, F, Steel, D, Kurian, M A, Radio, F C, Ferrero, G B, Carli, D, Tartaglia, M, Balci, T B, Powell-Hamilton, N N, Schrier Vergano, S A, Reutter, H, Hoefele, J, Günthner, R, Roeder, E R, Littlejohn, R O, Lessel, D, Lüttgen, S, Kentros, C, Anyane-Yeboa, K, Catarino, C B, Mercimek-Andrews, S, Denecke, J, Lyons, M J, Klopstock, T, Bhoj, E J, Bryant, L, Vanderver, A

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Recommending revised hepatoblastoma surveillance in children with a pathogenic ARID1A variant. Reply to “Cancer in ARID1A-Coffin-Siris syndrome: Review and report of a child with h... von van der Sluijs, P.J., Vergano, S.A., Roeder, E.R., Jongmans, M.C.J., Santen, G.W.E.

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Reproductive fitness in maternal homocystinuria due to cystathionine β‐synthase deficiency von Levy, H. L., Vargas, J. E., Waisbren, S. E., Kurczynski, T. W., Roeder, E. R., Schwartz, R. S., Rosengren, S., Prasad, C., Greenberg, C. R., Gilfix, B. M., MacGregor, D., Shih, V. E., Bao, L., Kraus, J. P.

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Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size von Shinawi, Marwan, Liu, Pengfei, Kang, Sung-Hae L, Shen, Joseph, Belmont, John W, Scott, Daryl A, Probst, Frank J, Craigen, William J, Graham, Brett H, Pursley, Amber, Clark, Gary, Lee, Jennifer, Proud, Monica, Stocco, Amber, Rodriguez, Diana L, Kozel, Beth A, Sparagana, Steven, Roeder, Elizabeth R, McGrew, Susan G, Kurczynski, Thaddeus W, Allison, Leslie J, Amato, Stephen, Savage, Sarah, Patel, Ankita, Stankiewicz, Pawel, Beaudet, Arthur L, Cheung, Sau Wai, Lupski, James R

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Loss-of-Function Mutations in the Human GLI2 Gene Are Associated with Pituitary Anomalies and Holoprosencephaly-like Features von Roessler, Erich, Du, Yang-Zhu, Mullor, Jose L., Casas, Esther, Allen, William P., Gillessen-Kaesbach, Gabriele, Roeder, Elizabeth R., Ming, Jeffrey E., Ariel Ruiz i Altaba, Muenke, Maximilian

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Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond–Blackfan anaemia von Wat, Margaret J, Enciso, Victoria B, Wiszniewski, Wojciech, Resnick, Trevor, Bader, Patricia, Roeder, Elizabeth R, Freedenberg, Debra, Brown, Chester, Stankiewicz, Pawel, Cheung, Sau-Wai, Scott, Daryl A

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Cataract in early onset and classic Cockayne syndrome von Ferreira, Rosane C., Roeder, Elizabeth R., Bateman, J. Bronwyn

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Mosaic trisomy 16 ascertained through amniocentesis: Evaluation of 11 new cases von Hsu, Wei-Tong, Shchepin, Dmitriy A., Mao, Rong, Berry-Kravis, Elizabeth, Garber, Ann P., Fischel-Ghodsian, Nathan, Falk, Rena E., Carlson, Dru E., Roeder, Elizabeth R., Leeth, Elizabeth A., Hajianpour, M.J., Wang, Jin-Chen C., Rosenblum-Vos, Lynne S., Bhatt, Sucheta D., Karson, Evelyn M., Hux, Charles H., Trunca, Carolyn, Bialer, Martin G., Linn, Sandra K., Schreck, Rhona R.

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Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndrome von Lin, Angela E., Semina, Elena V., Daack-Hirsch, Sandra, Roeder, Elizabeth R., Curry, Cynthia J.R., Rosenbaum, Kenneth, Weaver, David D., Murray, Jeffrey C.

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338 DELINEATION OF TWO SUBTLE CHROMOSOME DUPLICATIONS, 4p16 AND 22q11.2, IN A THREE-GENERATION FAMILY WITH MENTAL RETARDATION BY FLUORESCENT IN SITU HYBRIDIZATION AND ARRAY COMPARA... von Curry, C. J., Cotter, P. D., Roeder, E.R, Delozier, C. D., Clark, R. D., Drumheller, T., Rauen, K. A.

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Scapuloiliac dysostosis (Kosenow syndrome, pelvis-shoulder dysplasia) spectrum: Three additional cases von Elliott, Alison M., Roeder, Elizabeth R., Witt, David R., Rimoin, David L., Lachman, Ralph S.

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Brain Abnormalities in Patients with Germline Variants in H3F3: Novel Imaging Findings and Neurologic Symptoms Beyond Somatic Variants and Brain Tumors von Alves, CAPF, Sherbini, O, D'Arco, F, Steel, D, Kurian, MA, Radio, FC, Ferrero, GB, Carli, D, Tartaglia, M, Balci, TB, Powell-Hamilton, NN, Schrier Vergano, SA, Reutter, H, Hoefele, J, Günthner, R, Roeder, ER, Littlejohn, RO, Lessel, D, Lüttgen, S, Kentros, C, Anyane-Yeboa, K, Catarino, CB, Mercimek-Andrews, S, Denecke, J, Lyons, MJ, Klopstock, T, Bhoj, EJ, Bryant, L, Vanderver, A

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New brazing alloy eliminates metal-stress cracking von Huschler, E., Jr, Roeder, E. R.

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Van Allen Probes observation of localized drift resonance between poloidal mode ultra-low frequency waves and 60 keV electrons von Claudepierre, S. G., Mann, I. R., Takahashi, K., Fennell, J. F., Hudson, M. K., Blake, J. B., Roeder, J. L., Clemmons, J. H., Spence, H. E., Reeves, G. D., Baker, D. N., Funsten, H. O., W. Friedel, R. H., Henderson, M. G., Kletzing, C. A., Kurth, W. S., MacDowall, R. J., Smith, C. W., Wygant, J. R.

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Direct Recruitment of Polycomb Repressive Complex 1 to Chromatin by Core Binding Transcription Factors von Yu, Ming, Mazor, Tali, Huang, Hui, Huang, Hsuan-Ting, Kathrein, Katie L., Woo, Andrew J., Chouinard, Candace R., Labadorf, Adam, Akie, Thomas E., Moran, Tyler B., Xie, Huafeng, Zacharek, Sima, Taniuchi, Ichiro, Roeder, Robert G., Kim, Carla F., Zon, Leonard I., Fraenkel, Ernest, Cantor, Alan B.

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The Magnetic Electron Ion Spectrometer (MagEIS) Instruments Aboard the Radiation Belt Storm Probes (RBSP) Spacecraft von Blake, J. B., Carranza, P. A., Claudepierre, S. G., Clemmons, J. H., Crain, W. R., Dotan, Y., Fennell, J. F., Fuentes, F. H., Galvan, R. M., George, J. S., Henderson, M. G., Lalic, M., Lin, A. Y., Looper, M. D., Mabry, D. J., Mazur, J. E., McCarthy, B., Nguyen, C. Q., O’Brien, T. P., Perez, M. A., Redding, M. T., Roeder, J. L., Salvaggio, D. J., Sorensen, G. A., Spence, H. E., Yi, S., Zakrzewski, M. P.

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Gold nanoparticles as contrast agents in x-ray imaging and computed tomography von Cole, Lisa E, Ross, Ryan D, Tilley, Jennifer MR, Vargo-Gogola, Tracy, Roeder, Ryan K

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Alternating Morphology of the QRST Complex Preceding Sudden Death von RAEDER, EA, ROSENBAUM, DS, BHASIN, R, COHEN, RJ

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Role of SWI/SNF in acute leukemia maintenance and enhancer-mediated Myc regulation von Shi, Junwei, Whyte, Warren A, Zepeda-Mendoza, Cinthya J, Milazzo, Joseph P, Shen, Chen, Roe, Jae-Seok, Minder, Jessica L, Mercan, Fatih, Wang, Eric, Eckersley-Maslin, Melanie A, Campbell, Amy E, Kawaoka, Shinpei, Shareef, Sarah, Zhu, Zhu, Kendall, Jude, Muhar, Matthias, Haslinger, Christian, Yu, Ming, Roeder, Robert G, Wigler, Michael H, Blobel, Gerd A, Zuber, Johannes, Spector, David L, Young, Richard A, Vakoc, Christopher R

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