Refinement of a 400-kb Critical Region Allows Genotypic Differentiation between Isolated Lissencephaly, Miller-Dieker Syndrome, and Other Phenotypes Secondary to Deletions of 17p13... by Cardoso, Carlos, Leventer, Richard J., Ward, Heather L., Toyo-oka, Kazuhito, Chung, June, Gross, Alyssa, Martin, Christa L., Allanson, Judith, Pilz, Daniela T., Olney, Ann H., Mutchinick, Osvaldo M., Hirotsune, Shinji, Wynshaw-Boris, Anthony, Dobyns, William B., Ledbetter, David H.

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Case Report: Two Patients With Oculocerebrocutaneous Syndrome and Terminal Digital Amputations by Asher, Nathan G., MD, Olney, Ann H., MD, Schaefer, G. Bradley, MD

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Report of a patient with developmental delay, hearing loss, growth retardation, and cleft lip and palate and a deletion of 7q34-36.1: Review of distal 7q deletions by Rush, Eric T., Stevens, Jadd M., Sanger, Warren G., Olney, Ann H.

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Carriers and patients with muscle–eye–brain disease can be rapidly diagnosed by enzymatic analysis of fibroblasts and lymphoblasts by Vajsar, Jiri, Zhang, Wenli, Dobyns, William B., Biggar, Doug, Holden, Kenton R., Hawkins, Cynthia, Ray, Peter, Olney, Ann H., Burson, Catherine M., Srivastava, Anand K., Schachter, Harry

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Supine arm cycling during the post-flap recovery period for persons with spinal cord injuries: The multi-purpose arm cycle ergometer (M-PACE) safety and pilot testing by Olney, Christine M., Ferguson, John E., Voss, Greg, Nickel, Eric, Fairhurst, Stuart, Bornstein, Alexandra S., Kemmer, Sara, Stien, Crystal, Scheel, Kristin, Brenteson, Charlotte, Goding, Ann, Kruse, Mary Murphy, Eddy, Byron, Goldish, Gary, Hansen, Andrew H.

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Prenatal Diagnosis of Congenital Adrenal Hyperplasia Caused by P450 Oxidoreductase Deficiency by Reisch, Nicole, Idkowiak, Jan, Hughes, Beverly A, Ivison, Hannah E, Abdul-Rahman, Omar A, Hendon, Laura G, Olney, Ann Haskins, Nielsen, Shelly, Harrison, Rachel, Blair, Edward M, Dhir, Vivek, Krone, Nils, Shackleton, Cedric H. L, Arlt, Wiebke

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Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith–Wiedemann syndrome by Weksberg, Rosanna, Shuman, Cheryl, Caluseriu, Oana, Smith, Adam C., Fei, Yan-Ling, Nishikawa, Joy, Stockley, Tracy L., Best, Lyle, Chitayat, David, Olney, Ann, Ives, Elizabeth, Schneider, Adele, Bestor, Timothy H., Li, Madeline, Sadowski, Paul, Squire, Jeremy

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Clinical and volumetric changes with increasing functional impairment in familial frontotemporal lobar degeneration by Olney, Nicholas T., Ong, Elise, Goh, Sheng‐Yang M., Bajorek, Lynn, Dever, Reilly, Staffaroni, Adam M., Cobigo, Yann, Bock, Meredith, Chiang, Kevin, Ljubenkov, Peter, Kornak, John, Heuer, Hilary W., Wang, Ping, Rascovsky, Katya, Wolf, Amelia, Appleby, Brian, Bove, Jessica, Bordelon, Yvette, Brannelly, Patrick, Brushaber, Danielle, Caso, Christine, Coppola, Giovanni, Dickerson, Bradford C., Dickinson, Susan, Domoto‐Reilly, Kimiko, Faber, Kelly, Ferrall, Jessica, Fields, Julie, Fishman, Ann, Fong, Jamie, Foroud, Tatiana, Forsberg, Leah K., Gearhart, Debra J., Ghazanfari, Behnaz, Ghoshal, Nupur, Goldman, Jill, Graff‐Radford, Jonathan, Graff‐Radford, Neill R., Grant, Ian, Grossman, Murray, Haley, Dana, Hsiung, Gingyuek, Huey, Edward D., Irwin, David J., Jones, David T., Kantarci, Kejal, Karydas, Anna M., Kaufer, Daniel, Kerwin, Diana, Knopman, David S., Kramer, Joel H., Kraft, Ruth, Kremers, Walter, Kukull, Walter, Lapid, Maria I., Litvan, Irene, Mackenzie, Ian R., Maldonado, Miranda, Manoochehri, Masood, McGinnis, Scott M., McKinley, Emily C., Mendez, Mario F., Miller, Bruce L., Onyike, Chiadi, Pantelyat, Alex, Pearlman, Rodney, Petrucelli, Len, Potter, Madeleine, Rademakers, Rosa, Ramos, Eliana M., Rankin, Katherine P., Roberson, Erik D., Rogalski, Emily, Sengdy, Pheth, Shaw, Leslie M., Syrjanen, Jeremy, Tartaglia, M. Carmela, Tatton, Nadine, Taylor, Joanne, Toga, Arthur, Trojanowski, John Q., Weintraub, Sandra, Wong, Bonnie, Wszolek, Zbigniew, Boxer, Adam L., Boeve, Brad F., Rosen, Howard J.

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Array-based comparative genomic hybridization analysis of 1176 consecutive clinical genetics investigations by Pickering, Diane L., Eudy, James D., Olney, Ann Haskins, Dave, Bhavana J., Golden, Denae, Stevens, Jadd, Sanger, Warren G.

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Vital Signs: Update on Zika Virus–Associated Birth Defects and Evaluation of All U.S. Infants with Congenital Zika Virus Exposure — U.S. Zika Pregnancy Registry, 2016 by Reynolds, Megan R., Jones, Abbey M., Petersen, Emily E., Lee, Ellen H., Rice, Marion E., Bingham, Andrea, Ellington, Sascha R., Evert, Nicole, Reagan-Steiner, Sarah, Oduyebo, Titilope, Brown, Catherine M., Martin, Stacey, Ahmad, Nina, Bhatnagar, Julu, Macdonald, Jennifer, Gould, Carolyn, Fine, Anne D., Polen, Kara D., Lake-Burger, Heather, Hillard, Christina L., Hall, Noemi, Yazdy, Mahsa M., Slaughter, Karnesha, Sommer, Jamie N., Adamski, Alys, Raycraft, Meghan, Fleck-Derderian, Shannon, Gupta, Jyoti, Newsome, Kimberly, Baez-Santiago, Madelyn, Slavinski, Sally, White, Jennifer L., Moore, Cynthia A., Shapiro-Mendoza, Carrie K., Petersen, Lyle, Boyle, Coleen, Jamieson, Denise J., Meaney-Delman, Dana, Honein, Margaret A.

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Inherited 14q duplication and 21q deletion: A rare adjacent‐2 segregation in multiple family members by Dave, Bhavana J., Olney, Ann Haskins, Zaleski, Dianna H., Pickering, Diane L., Becker, Troy A., Chipman, Hope E., Sanger, Warren G.

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Informed consent for medical photographs by Cunniff, Christopher, Byrne, Janice L.B., Hudgins, Louanne M., Moeschler, John B., Olney, Ann Haskins, Pauli, Richard M., Seaver, Lauri H., Stevens, Cathy A., Figone, Christopher

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Cryptic duplication and deletion of 9q34.3 → qter in a family with a t(9;22)(q34.3;p11.2) by Sanger, Travis M., Olney, Ann Haskins, Zaleski, Dianna, Pickering, Diane, Nelson, Marilu, Sanger, Warren G., Dave, Bhavana J.

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Velocardiofacial Syndrome (Shprintzen Syndrome, Chromosome 22q11 Deletion Syndrome) by Olney, Ann Haskins, Kolodziej, Peg

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Congenital microgastria and limb reduction defects by CUNNIFF, C, WILLIAMSON-KRUSE, L, OLNEY, A. H

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Waardenburg Syndrome by Smith, Shelley, Kolodziej, Peg, Olney, Ann Haskins

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Hypothalamic dysfunction with polydactyly and hypoplastic nails by Schaefer, G. Bradley, Olney, Ann Haskins, Bodensteiner, John

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Branchio-oto-renal Syndrome (BOR Syndrome, Melnick-Fraser Syndrome) by Olney, Ann Haskins, Kolodziej, Peg

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Pallister-Hall Syndrome by Olney, Ann Haskins, Kolodziej, Peg

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Turner Syndrome by Olney, Ann Haskins, Schaefer, G. Bradley

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