Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndrome von Tan, T Y, Aftimos, S, Worgan, L, Susman, R, Wilson, M, Ghedia, S, Kirk, E P, Love, D, Ronan, A, Darmanian, A, Slavotinek, A, Hogue, J, Moeschler, J B, Ozmore, J, Widmer, R, Savarirayan, R, Peters, G

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Two arginine rich domains in the p14ARF tumour suppressor mediate nucleolar localization von RIZOS, H, DARMANIAN, A. P, MANN, G. J, KEFFORD, R. F

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A melanoma-associated germline mutation in exon 1β inactivates p14ARF von RIZOS, Helen, PUIG, Susana, BADENAS, Celia, MALVEHY, Josep, DARMANIAN, Artur P, JIMENEZ, Loli, MILA, Montserrat, KEFFORD, Richard F

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Clinical trial design during and beyond the pandemic: the I-SPY COVID trial von Calfee, Carolyn S., Liu, Kathleen D., Asare, Adam L., Beitler, Jeremy R., Berger, Paul A., Coleman, Melissa H., Crippa, Alessio, Discacciati, Andrea, Eklund, Martin, Files, Daniel C., Gandotra, Sheetal, Gibbs, Kevin W., Henderson, Paul, Levitt, Joseph E., Lu, Ruixiao, Matthay, Michael A., Meyer, Nuala J., Russell, Derek W., Thomas, Karl W., Esserman, Laura J., Mittel, Aaron M., Dzierba, Amy L., Madahar, Purnema, Serra, Alexis L., Rosen, Amanda, Garcia, Ivan, Muir, Justin, Schicchi, John, Darmanian, Anita, Wahab, Romina, Gosek, Katarzyna, Auld, Sara C., Adelman, Max W., Nugent, Katherine L., Harris, Gavin H., Creel-Bulos, Christina, Yang, Philip, Detelich, Joshua F., Spainhour, Christine, Cobb, Nathan K., Sonti, Rajiv, Orr, Lindsey A., Robinson, Philip A., Sarafian, Farjad, Martinez, Esmeralda, Jones, Patrice, Nguyen, Julie, Obermiller, Timothy F., Weiler-Lisowski, Bethany, Kufa, Lucia, Saba, Paul L., Wyatt, Jaime, Youssef, Fady A., Tanios, Maged, Blevins, Daniel, Macias, Laura R., Suarez, Alexis E., Reyes, Maria B., Jung, Michelle, Melendrez, Marylee, Rosario-Remigio, Lissette, Su, Henry, Friedman, Eliot B., Angelucci, Christina M., Chaparro-Rojas, Fredy, Sternlieb, Mitchell P., Sutter, Jacqueline B., Whealon, Spencer, Nair, Rahul, Lopez, Brenda, Amosu, Omowunmi, Tzehaie, Hiwet, Wunderink, Richard G., Patel, Chirag, Simonson, Austin, Dodin, Jamal, Oliver, Tony, Lupu, Roxana A., Meyers, Michelle, Albertson, Timothy E., Haczku, Angela, Hardy, Erin, Morrissey, Brian M., Juarez, Maya M., Pearson, Skyler J., Lee, Richard Anthony, Amin, Alpesh N., Jauregui, Alejandra, Fields, Scott, Ng, Diana, Daniel, Brian M., Yee, Kimberly, Jones, Chayse, Burnham, Ellen L., McKeehan, Jeffrey D., Ittner, Caroline A. G., Reilly, John P., Mangalmurti, Nilam S., Rodrigues, Laura G., Weisman, Ariel R.

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Prader-Willi syndrome phenocopy due to duplication of Xq21.1-q21.31, with array CGH of the critical region von Gabbett, MT, Peters, GB, Carmichael, JM, Darmanian, AP, Collins, FA

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Novel subtypes of severe COVID-19 respiratory failure based on biological heterogeneity: a secondary analysis of a randomized controlled trial von Alipanah-Lechner, Narges, Hurst-Hopf, James, Delucchi, Kevin, Swigart, Lamorna, Willmore, Andrew, LaCombe, Benjamin, Dewar, Robin, Lane, H Clifford, Lallemand, Perrine, Liu, Kathleen D, Esserman, Laura, Matthay, Michael A, Calfee, Carolyn S

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I-SPY COVID adaptive platform trial for COVID-19 acute respiratory failure: rationale, design and operations von Files, Daniel Clark, Calfee, Carolyn S, Asare, Adam L, Beitler, Jeremy R, Berger, Paul A, Burnham, Ellen L, Cimino, George, Coleman, Melissa H, Crippa, Alessio, Discacciati, Andrea, Gandotra, Sheetal, Ittner, Caroline A G, Jauregui, Alejandra, Khan, Kashif T, Koff, Jonathan L, Levitt, Joe, Lu, Ruixiao, McKeehan, Jeffrey D, Meyer, Nuala J, Russell, Derek W, Thomas, Karl W, Esserman, Laura J, Liu, Kathleen D, Liu, Kathleen D, Matthay, Michael A, Beitler, Jeremy R, Asare, Adam L, Yen, Albert F, Jauregui, Alejandra, Crippa, Alessio, Rosen, Amanda, Dzierba, Amy L, Discacciati, Andrea, Haczku, Angela, Barker, Anna D, Weisman, Ariel R, Daniel, Brian M, Morrissey, Brian M, Jones, Chayse, Files, Daniel C, Russell, Derek W, Ng, Diana, Burnham, Ellen L, Youssef, Fady A, Chaparro-Rojas, Fredy, Barot, Harsh V, Su, Heny, Sutter, Jacqueline B, Dodin, Jamal, Lee, Jerry S, Kazianis, John, Koff, Jonathan L, Detelich, Joshua F, Lang, Julie E, Thomas, Karl W, Gosek, Katarzyna, Nugent, Katherine L, Yee, Kimberly, Rodrigues, Laura G, Orr, Lindsey A, Rosario-Remigio, Lissette, Huerta, Luis E, Reyes, Maria B, Eklund, Martin, LaRose, Mary, Adelman, Max W, Juarez, Maya M, Jung, Michelle, Cobb, Nathan K, Aggarwal, Neil, Berger, Paul A, Saban, Paul L, Marshall, Peter S, Robinson, Philiip A, Yang, Philip, Madahar, Purnema, Nair, Rahul, Wunderink, Richard G, Wahab, Romina, Lupu, Roxana A, Lu, Ruixiao, Kumar, Santhi I, Auld, Sara C, Fields, Scott, Gandotra, Sheetal, Whealon, Spencer, Albertson, Timothy E, Obermiller, Timothy F, Oliver, Tony, Schicchi, John, Sarafian, Farjad, Nguyen, Julie, Blevins, Daniel, Melendrez, Marylee, Tzehaie, Hiwet, Amosu, Omowunmi, Levitt, Joe, Peterfreund, Gregory, Landreth, Leigha, Parks, Lisa

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C52 ILLUSTRATIVE DISEASE PRESENTATIONS IN CRITICAL CARE I: Spontaneous Retropharyngeal And Mediastinal Hemorrhage Associated With Wild-Type Transthyretin Systemic Amyloidosis von Cummings, M J, Katz, S E, De Gonzalez, A Koehne, Darmanian, A C, O'Donnell, M R

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Multiple abnormalities of the p16INK4a-pRb regulatory pathway in cultured melanoma cells von Rizos, H, Darmanian, A P, Indsto, J O, Shannon, J A, Kefford, R F, Mann, G J

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Prader-Willi syndrome phenocopy due to duplication of Xq21. 1-q21.31, with array CGH of the critical region von GABBETT, M. T, PETERS, G. B, CARMICHAEL, J. M, DARMANIAN, A. P, COLLINS, F. A

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Issues arising from the prenatal diagnosis of some rare trisomy mosaics-the importance of cryptic fetal mosaicism von Daniel, Art, Wu, Zhanhe, Darmanian, Artur, Malafiej, Paul, Tembe, Varsha, Peters, Greg, Kennedy, Craig, Adès, Lesley

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Three different origins for apparent triploid/diploid mosaics von Daniel, Art, Wu, Zhanhe, Darmanian, Artur, Collins, Felicity, Jackson, Julianne

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Recombinants of intrachromosomal transposition of subtelomeres in chromosomes 1 and 2: A cause of minute terminal chromosomal imbalances von Daniel, Art, Baker, Elizabeth, Chia, Nicole, Haan, Eric, Malafiej, Paul, Hinton, Lyn, Clarke, Nigel, Adès, Lesley, Darmanian, Artur, Callen, David

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Mutations in the INK4a/ARF Melanoma Susceptibility Locus Functionally Impair p14 super(ARF) von Rizos, H, Darmanian, A P, Holland, E A, Mann, G J, Kefford, R F

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Mutations in the INK4a/ARF Melanoma Susceptibility Locus Functionally Impair p14ARF von Rizos, Helen, Darmanian, Artur P., Holland, Elizabeth A., Mann, Graham J., Kefford, Richard F.

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A melanoma-associated germline mutation in exon 1beta inactivates p14ARF von Rizos, H, Puig, S, Badenas, C, Malvehy, J, Darmanian, A P, Jiménez, L, Milà, M, Kefford, R F

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Analysis of CDKN2A. CDKN2B, P16??, P21 and CDK4 in melanoma cells: 471 von Rizos, H, Darmanian, A, Shannon, J A, Kefford, R F, Mann, G J

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Dynamics of solitons in coupled optical fibers von ABDULLAEV, F. K, ABRAROV, R. M, DARMANYAN, S. A

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Neuroblastoma Molecular Risk-Stratification of DNA Copy Number and ALK Genotyping via Cell-Free Circulating Tumor DNA Profiling von Kahana-Edwin, Smadar, Cain, Lucy E., McCowage, Geoffrey, Darmanian, Artur, Wright, Dale, Mullins, Anna, Saletta, Federica, Karpelowsky, Jonathan

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SNP chromosome microarray genotyping for detection of uniparental disomy in the clinical diagnostic laboratory von Ngo, Con, Baluyot, Maria, Bennetts, Bruce, Carmichael, Johanna, Clark, Alissa, Darmanian, Artur, Gayagay, Thet, Jones, Luke, Nash, Benjamin, Clark, Melanie, Jose, Ngaire, Robinson, Samantha, St Heaps, Luke, Wright, Dale

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