Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing von Zarate, Yuri A., Perry, Hazel, Ben-Omran, Tawfeg, Sellars, Elizabeth A., Stein, Quinn, Almureikhi, Mariam, Simmons, Kirk, Klein, Ophir, Fish, Jennifer, Feingold, Murray, Douglas, Jessica, Kruer, Michael C., Si, Yue, Mao, Rong, McKnight, Dianalee, Gibellini, Federica, Retterer, Kyle, Slavotinek, Anne

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Application of full-genome analysis to diagnose rare monogenic disorders von Shieh, Joseph T., Penon-Portmann, Monica, Wong, Karen H. Y., Levy-Sakin, Michal, Verghese, Michelle, Slavotinek, Anne, Gallagher, Renata C., Mendelsohn, Bryce A., Tenney, Jessica, Beleford, Daniah, Perry, Hazel, Chow, Stephen K., Sharo, Andrew G., Brenner, Steven E., Qi, Zhongxia, Yu, Jingwei, Klein, Ophir D., Martin, David, Kwok, Pui-Yan, Boffelli, Dario

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Publisher Correction: Application of full-genome analysis to diagnose rare monogenic disorders von Shieh, Joseph T., Penon-Portmann, Monica, Wong, Karen H. Y., Levy-Sakin, Michal, Verghese, Michelle, Slavotinek, Anne, Gallagher, Renata C., Mendelsohn, Bryce A., Tenney, Jessica, Beleford, Daniah, Perry, Hazel, Chow, Stephen K., Sharo, Andrew G., Brenner, Steven E., Qi, Zhongxia, Yu, Jingwei, Klein, Ophir D., Martin, David, Kwok, Pui-Yan, Boffelli, Dario

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Genetic Testing in Craniofacial Care: Development of Algorithms for Testing Patients with Orofacial Clefting, Branchial Arch Anomalies, and Craniosynostosis von Gallagher, Emily R, Chow, Penny, Mills, Maria R, Perry, Hazel, Tam, Allison C, Rosenbluth, Glenn, Gutierrez, Yvonne R, Shamshoni, Jessica Kianmahd, Matthews, Marisa, Schweitzer, Daniela N, Hing, Anne

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DLX4 is associated with orofacial clefting and abnormal jaw development von Wu, Di, Mandal, Shyamali, Choi, Alex, Anderson, August, Prochazkova, Michaela, Perry, Hazel, Gil-Da-Silva-Lopes, Vera L, Lao, Richard, Wan, Eunice, Tang, Paul Ling-Fung, Kwok, Pui-yan, Klein, Ophir, Zhuan, Bian, Slavotinek, Anne M

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Case Report of Floating-Harbor Syndrome With Bilateral Cleft Lip von Ko, Jaemin, Pomerantz, Jason H., Perry, Hazel, Shieh, Joseph T., Slavotinek, Anne M., Oberoi, Snehlata, Klein, Ophir D.

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A novel EFNB1 mutation (c.712delG) in a family with craniofrontonasal syndrome and diaphragmatic hernia von Hogue, Jacob, Shankar, Suma, Perry, Hazel, Patel, Reena, Vargervik, Karin, Slavotinek, Anne

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Application of full-genome analysis to diagnose rare monogenic disorders (vol 6, 77, 2021) von Shieh, Joseph T., Penon-Portmann, Monica, Wong, Karen H. Y., Levy-Sakin, Michal, Verghese, Michelle, Slavotinek, Anne, Gallagher, Renata C., Mendelsohn, Bryce A., Tenney, Jessica, Beleford, Daniah, Perry, Hazel, Chow, Stephen K., Sharo, Andrew G., Brenner, Steven E., Qi, Zhongxia, Yu, Jingwei, Klein, Ophir D., Martin, David, Kwok, Pui-Yan, Boffelli, Dario

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An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discovery von Haghighi, Alireza, Krier, Joel B., Toth-Petroczy, Agnes, Cassa, Christopher A., Frank, Natasha Y., Carmichael, Nikkola, Fieg, Elizabeth, Bjonnes, Andrew, Mohanty, Anwoy, Briere, Lauren C., Lincoln, Sharyn, Lucia, Stephanie, Gupta, Vandana A., Söylemez, Onuralp, Sutti, Sheila, Kooshesh, Kameron, Qiu, Haiyan, Fay, Christopher J., Perroni, Victoria, Valerius, Jamie, Hanna, Meredith, Frank, Alexander, Ouahed, Jodie, Snapper, Scott B., Pantazi, Angeliki, Chopra, Sameer S., Leshchiner, Ignaty, Stitziel, Nathan O., Feldweg, Anna, Mannstadt, Michael, Loscalzo, Joseph, Sweetser, David A., Liao, Eric, Stoler, Joan M., Nowak, Catherine B., Sanchez-Lara, Pedro A., Klein, Ophir D., Perry, Hazel, Patsopoulos, Nikolaos A., Raychaudhuri, Soumya, Goessling, Wolfram, Green, Robert C., Seidman, Christine E., MacRae, Calum A., Sunyaev, Shamil R., Maas, Richard L., Vuzman, Dana

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Cover Image, Volume 176A, Number 4, April 2018 von Zarate, Yuri A., Smith‐Hicks, Constance L., Greene, Carol, Abbott, Mary‐Alice, Siu, Victoria M., Calhoun, Amy R. U. L., Pandya, Arti, Li, Chumei, Sellars, Elizabeth A., Kaylor, Julie, Bosanko, Katherine, Kalsner, Louisa, Basinger, Alice, Slavotinek, Anne M., Perry, Hazel, Saenz, Margarita, Szybowska, Marta, Wilson, Louise C., Kumar, Ajith, Brain, Caroline, Balasubramanian, Meena, Dubbs, Holly, Ortiz‐Gonzalez, Xilma R., Zackai, Elaine, Stein, Quinn, Powell, Cynthia M., Schrier Vergano, Samantha, Britt, Allison, Sun, Angela, Smith, Wendy, Bebin, E. Martina, Picker, Jonathan, Kirby, Amelia, Pinz, Hailey, Bombei, Hannah, Mahida, Sonal, Cohen, Julie S., Fatemi, Ali, Vernon, Hilary J., McClellan, Rebecca, Fleming, Leah R., Knyszek, Brittney, Steinraths, Michelle, Velasco Gonzalez, Cruz, Beck, Anita E., Golden‐Grant, Katie L., Egense, Alena, Parikh, Aditi, Raimondi, Chantalle, Angle, Brad, Allen, William, Schott, Suzanna, Algrabli, Adi, Robin, Nathaniel H., Ray, Joseph W., Everman, David B., Gambello, Michael J., Chung, Wendy K.

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Novel FGFR2 deletion in a patient with Beare-Stevenson-like syndrome von Slavotinek, Anne, Crawford, Howard, Golabi, Mahin, Tao, Cathy, Perry, Hazel, Oberoi, Sneha, Vargervik, Karin, Friez, Michael

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Clefting in trisomy 9p patients: genotype-phenotype correlation using microarray comparative genomic hybridization von Jelin, Angie, Perry, Hazel, Hogue, Jacob, Oberoi, Snehlata, Cotter, Philip D, Klein, Ophir D

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A novel EFNB1 mutation (c.712delG) in a family with craniofrontonasal syndrome and diaphragmatic hernia von Hogue, Jacob, Shankar, Suma, Perry, Hazel, Patel, Reena, Vargervik, Karin, Slavotinek, Anne

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Self-Sensing Rubber for Bridge Bearing Monitoring von Orfeo, Alessandra, Tubaldi, Enrico, McAlorum, Jack, Perry, Marcus, Ahmadi, Hamid, McDonald, Hazel

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Language in popular American culture constructs the meaning of healthy and unhealthy eating: Narratives of craveability, excitement, and social connection in movies, television, so... von Turnwald, Bradley P., Perry, Margaret A., Jurgens, David, Prabhakaran, Vinodkumar, Jurafsky, Dan, Markus, Hazel R., Crum, Alia J.

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Current practices of health care providers in recommending online resources for chronic pain self-management von Devan, Hemakumar, Godfrey, Hazel K, Perry, Meredith A, Hempel, Dagmar, Saipe, Barbara, Hale, Leigh, Grainger, Rebecca

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What makes palliative care needs "complex"? A multisite sequential explanatory mixed methods study of patients referred for specialist palliative care von Finucane, Anne M., Swenson, Connie, MacArtney, John I., Perry, Rachel, Lamberton, Hazel, Hetherington, Lucy, Graham-Wisener, Lisa, Murray, Scott A., Carduff, Emma

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Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer von Ruark, Elise, Snape, Katie, Humburg, Peter, Loveday, Chey, Bajrami, Ilirjana, Brough, Rachel, Rodrigues, Daniel Nava, Renwick, Anthony, Seal, Sheila, Ramsay, Emma, Duarte, Silvana Del Vecchio, Rivas, Manuel A., Warren-Perry, Margaret, Zachariou, Anna, Campion-Flora, Adriana, Hanks, Sandra, Murray, Anne, Pour, Naser Ansari, Douglas, Jenny, Gregory, Lorna, Rimmer, Andrew, Walker, Neil M., Yang, Tsun-Po, Adlard, Julian W., Barwell, Julian, Berg, Jonathan, Brady, Angela F., Brewer, Carole, Brice, Glen, Chapman, Cyril, Cook, Jackie, Davidson, Rosemarie, Donaldson, Alan, Douglas, Fiona, Eccles, Diana, Evans, D. Gareth, Greenhalgh, Lynn, Henderson, Alex, Izatt, Louise, Kumar, Ajith, Lalloo, Fiona, Miedzybrodzka, Zosia, Morrison, Patrick J., Paterson, Joan, Porteous, Mary, Rogers, Mark T., Shanley, Susan, Walker, Lisa, Gore, Martin, Houlston, Richard, Brown, Matthew A., Caufield, Mark J., Deloukas, Panagiotis, McCarthy, Mark I., Todd, John A., Turnbull, Clare, Reis-Filho, Jorge S., Ashworth, Alan, Antoniou, Antonis C., Lord, Christopher J., Donnelly, Peter, Rahman, Nazneen

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The positive impact of interprofessional education: a controlled trial to evaluate a programme for health professional students von Darlow, Ben, Coleman, Karen, McKinlay, Eileen, Donovan, Sarah, Beckingsale, Louise, Gray, Ben, Neser, Hazel, Perry, Meredith, Stanley, James, Pullon, Sue

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Arts-based approaches to promoting health in sub-Saharan Africa: a scoping review von Bunn, Christopher, Kalinga, Chisomo, Mtema, Otiyela, Abdulla, Sharifa, Dillip, Angel, Lwanda, John, Mtenga, Sally M, Sharp, Jo, Strachan, Zoë, Gray, Cindy M, Crampin, Amelia, Gill, Jason, Gray, Stuart, Namadingo, Hazel, Perry, Mia, Todd, Helen

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