BURNER FOR GAS TURBINE ENGINE von FISHER, EARL R, GREENBERG, PAUL B

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Folded-over pilot burner von FISHER, EARL R, GREENBERG, PAUL B

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Thermal expansion means for combustion chambers von ROBIN CHARLES D, HURD RICHARD C, FISHER EARL R

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Lightweight Ship Propulsion Systems. Part III. System Alternatives and Critical Technologies von Kuo ,Simion C, Horton ,Travis L O, Deane ,Charles W, Shu ,Ho-Tien, Fisher,Earl R

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Early Surgical Therapy for Drug-Resistant Temporal Lobe Epilepsy: A Randomized Trial von Engel, Jerome, McDermott, Michael P, Wiebe, Samuel, Langfitt, John T, Stern, John M, Dewar, Sandra, Sperling, Michael R, Gardiner, Irenita, Erba, Giuseppe, Fried, Itzhak, Jacobs, Margaret, Vinters, Harry V, Mintzer, Scott, Kieburtz, Karl, Early Randomized Surgical Epilepsy Trial (ERSET) Study Group, for the

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The Lancet Breast Cancer Commission: tackling a global health, gender, and equity challenge von Coles, Charlotte Elizabeth, Anderson, Benjamin O, Cameron, David, Cardoso, Fatima, Horton, Richard, Knaul, Felicia Marie, Mutebi, Miriam, Lee, Naomi, Abraham, Jean E, Anderson, Benjamin O, André, Fabrice, Barrios, Carlos H, Bliss, Judith M, Boughey, Judy C, Cameron, David A, Cardoso, Fatima V, Carey, Lisa A, Chatterjee, Sanjoy, Coles, Charlotte E, Cuzick, Jack, Du Plooy, Dorothy, Francis, Prudence A, Gralow, Julie R, Jagsi, Reshma, Knaul, Felicia M, Ma, Fei, Mann, Ritse M, McIntosh, Stuart A, Mertz, Shirley A, Mutebi, Miriam, Olopade, Funmi, Phillips, Kelly-Anne, Poortmans, Philip M, Spanic, Tanja, Spence, Dingle, Stobart, Hilary, Symmans, Fraser WF, Villarreal-Garza, Cynthia, Yip, Cheng-Har, Bienz, Maya J, Drewett, Lynsey M, Fulton, Alex, Inbah Rajah, Dharrnesha, Kazmi, Farasat, Rubasingham, Jeffrey, Thompson, Mareike, Vargas, Valentina, Arreola, Hector, Badwe, Raj A, Calderon Anyosa, Renzo JC, Dave, Rajiv V, De-Graft Aikins, Ama, Earl, Helena M, Essue, Beverley M, Etzioni, Ruth B, Hawley, Sarah T, Jiang, Xiaoxiao, Mittra, Indraneel, Moreno, Patricia I, Nargund, Renu Sara, Noble, Cara, Smith, Robert A, Verhoeven, Didier, Wang, Jiani N, Watkins, David A, Zikmund-Fisher, Brian J

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Bridging disciplines: An evaluation of learning about Interprofessional roles and responsibilities through an interactive group activity von Earl, Sally, Thweatt, Lesley, Parkes, Emmy, Fisher, Amy, Higdon, Carolyn, Shirley, Heather Landry, Wehring, Susan P., Lim, Younghee, Lirette, Seth T., Adcock, Kim G.

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Large-scale mutational analysis identifies UNC93B1 variants that drive TLR-mediated autoimmunity in mice and humans von Rael, Victoria E, Yano, Julian A, Huizar, John P, Slayden, Leianna C, Weiss, Madeleine A, Turcotte, Elizabeth A, Terry, Jacob M, Zuo, Wenqi, Thiffault, Isabelle, Pastinen, Tomi, Farrow, Emily G, Jenkins, Janda L, Becker, Mara L, Wong, Stephen C, Stevens, Anne M, Otten, Catherine, Allenspach, Eric J, Bonner, Devon E, Bernstein, Jonathan A, Wheeler, Matthew T, Saxton, Robert A, Liu, Bo, Majer, Olivia, Barton, Gregory M

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De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation von Mao, Dongxue, Reuter, Chloe M., Farrow, Emily G., Rosenfeld, Jill A., Mackenzie, Katherine M., Küry, Sébastien, Genetti, Casie A., Alejandro, Mercedes, Agrawal, Pankaj B., Alvey, Justin, Ashley, Euan A., Balasubramanyam, Ashok, Beck, Anita, Bellen, Hugo J., Berg-Rood, Beverly, Bernier, Raphael, Bivona, Stephanie, Bohnsack, John, Briere, Lauren C., Burke, Elizabeth A., Butte, Manish J., Carrasquillo, Olveen, Cogan, Joy D., Cole, F. Sessions, Colley, Heather A., Cooper, Cynthia M., Craigen, William J., Cunningham, Michael, Dasari, Surendra, Dayal, Jyoti G., Dhar, Shweta U., Emrick, Lisa T., Estwick, Tyra, Ferreira, Carlos, Fieg, Elizabeth L., Fogel, Brent L., Forghani, Irman, Gahl, William A., Godfrey, Rena A., Goldman, Alica M., Hahn, Sihoun, Hanchard, Neil A., Hing, Anne, Holm, Ingrid A., Huang, Yong, Jamal, Fariha, Jayadev, Suman, Karaviti, Lefkothea, Kelley, Emily G., Kohane, Isaac S., Kohler, Jennefer N., Krakow, Deborah, Korrick, Susan, Koziura, Mary, Krier, Joel B., Lam, Byron, Lanpher, Brendan C., Lanza, Ian R., Lee, Brendan H., Lewis, Richard A., Loo, Sandra K., Majcherska, Marta M., Malicdan, May Christine V., Mamounas, Laura A., Markello, Thomas C., Martin, Martin G., Martínez-Agosto, Julian A., McCormack, Colleen E., Merritt, J. Lawrence, Moretti, Paolo M., Mulvihill, John J., Murdock, David R., Nickerson, Deborah, Pallais, J. Carl, Posey, Jennifer E., Potocki, Lorraine, Raja, Archana N., Renteria, Genecee, Rosenfeld, Jill A., Samson, Susan L., Schedl, Timothy, Shakachite, Lisa, Signer, Rebecca, Silverman, Edwin K., Sybert, Virginia, Tekin, Mustafa, Thorson, Willa, Tran, Alyssa A., Urv, Tiina K., Wahl, Colleen E., Wegner, Daniel, Wheeler, Matthew T., Yamamoto, Shinya, Yang, John, Yoon, Amanda J., Yu, Guoyun, Zastrow, Diane B., Zhao, Chunli, Bernstein, Jonathan A., Chao, Hsiao-Tuan

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Model organisms contribute to diagnosis and discovery in the undiagnosed diseases network: current state and a future vision von Baldridge, Dustin, Wangler, Michael F, Bowman, Angela N, Yamamoto, Shinya, Schedl, Tim, Pak, Stephen C, Postlethwait, John H, Shin, Jimann, Solnica-Krezel, Lilianna, Bellen, Hugo J, Westerfield, Monte

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Early-Life Outcomes in Relation to Social Determinants of Health for Children Born Extremely Preterm von Bell, Edward F., Alksninis, Barbara, Hoffman, Laurie, Leach, Teresa M., Ventura, Suzy, Hibbs, Anna Maria, Walsh, Michele C., Yalcinkaya, Gulgun, Holmes, Anne, Johnson, Kathy, Beiersdorfer, Traci, Fischer, Estelle E., Hessling, Jody, Malcolm, William F., Grimes, Sandra, Gustafson, Kathryn E., Bose, Gennie, Rhodes-Ryan, Ginger, Patel, Ravi M., Carlton, David P., Bottcher, Diane I., Higgins, Rosemary D., Smiley, Lucy, Duncan, Andrea, Stephens, Emily K., Allain, Elizabeth, Green, Charles, Jones, Patrick M., Morris, Brenda H., Wright, Sharon L., Nelin, Leif D., Slaughter, Jonathan L., Fortney, Christine A., Levengood, Katelyn, Batterson, Nancy, Sullivan, Rox Ann, Fowler, Aubrey, Tonneman, Jill, Chao, Michelle, Beckford, Demi R., Baugher, Hallie, Hanlon, Cory, McCool, Jacqueline, Bann, Carla M., Crawford, Margaret M., Bentley, Barbara, Bruno, Elizabeth, Palmquist, Andrew W., Proud, Melinda S., John, Nicholas H. St, Wager, Natalie, Church, Paige T., Sibley, Cecelia E., Nelson, Kathleen G., Preskitt, Julie, Purdy, Isabell B., Vaucher, Yvonne E., Bell, Edward F., Colaizy, Tarah T., Widness, John A., Goeke, Claire A., Walker, Jacky R., Henning, Megan M., Ellsbury, Dan L., Bauer, Charles R., Calejo, Maria, Berkowits, Michelle Harwood, Watterberg, Kristi L., Catts, Christine, Vangala, Saritha, Boylin, Elizabeth, Maffett, Deanna, Sabaratnam, Premini, Scorsone, Ann Marie, Wadkins, Holly I.M., Yost, Kelley, Li, Emily, Brion, Luc P., Heyne, Roy J., Adams, Sally S., Guzman, Alicia, Heyne, Elizabeth T., McDougald, E. Rebecca, Morgan, Janet S., Minton, Stephen D., Sheffield, Mark J., Rau, Carrie A., Jordan, Jamie, Steffen, Michael, Weaver-Lewis, Kimberlee, Zanetti, Karen, Jackson, Barbara G., Halfond, Raquel, Waldrep, Ellen L., Shankaran, Seetha, Panaitescu, Bogdan, Wiggins, Stephanie A., Jacobs, Harris, Butler, Christine G., Romano, Elaine

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Bi-allelic variants in INTS11 are associated with a complex neurological disorder von Tepe, Burak, Cogne, Benjamin, Neil, Jennifer E., Walsh, Christopher A., Magal, Nurit, Drasinover, Valerie, Schwab, Tanya, Schmitz, Chris, Clark, Karl, Blanc, Pierre, Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin, Bayrak-Toydemir, Pinar, Beck, Anita, Behrens, Edward, Bican, Anna, Bivona, Stephanie, Blue, Elizabeth, Boyd, Brenna, Briere, Lauren C., Brown, Gabrielle, Byers, Peter, Byrd, William E., Carey, John, Clark, Gary D., Coakley, Terra R., Colley, Heather A., Craigen, William J., Cunningham, Michael, Dasari, Surendra, Dayal, Jyoti G., Deardorff, Matthew, Dipple, Katrina, Doherty, Daniel, Doss, Argenia L., Emrick, Lisa T., Fernandez, Liliana, Forghani, Irman, Glass, Ian, Gochuico, Bernadette, Golden-Grant, Katie, Goldrich, Madison P., Gutierrez, Irma, Hamid, Rizwan, Hayes, Nichole, Hom, Jason, Horike-Pyne, Martha, Isasi, Rosario, Jarvik, Jeffrey, Jobanputra, Vaidehi, Karaviti, Lefkothea, Kiley, Dana, Kobren, Shilpa N., Krasnewich, Donna M., LeBlanc, Kimberly, Levitt, Roy, Mahoney, Rachel, Malicdan, May Christine V., Mamounas, Laura A., Mao, Rong, Maravilla, Kenneth, Marom, Ronit, Martin, Martin G., Martínez-Agosto, Julian A., Merritt, J. Lawrence, Morava, Eva, Newman, John H., Nickerson, Deborah, Novacic, Donna, Oglesbee, Devin, Pace, Laura, Palmer, Christina GS, Papp, Jeanette C., Rao, Deepak A., Renteria, Genecee, Reuter, Chloe M., Robertson, Amy K., Rosenfeld, Jill A., Rossignol, Francis, Ruzhnikov, Maura, Scott, C. Ron, Shin, Jimann, Sinsheimer, Janet S., Sullivan, Jennifer A., Sun, Angela, Tabor, Holly K., Telischi, Fred, Toro, Camilo, Tucker, Brianna M., Urv, Tiina K., Vogel, Tiphanie P., Walker, Melissa, Wangler, Michael F., Perry, Katherine Wesseling, Westerfield, Monte, Wolfe, Lynne A., Worley, Kim, Xiao, Changrui, Zuchner, Stephan

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A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3 von Michener, Sydney L., Chan, Hiuling, Rosenfeld, Jill A., Bekheirnia, Mir Reza, Wagner, Matias, Engels, Hartmut, Guillen Sacoto, Maria J., McDonnell, Pamela P., Pastinen, Tomi, Zhou, Dihong, Bolton, Jeffrey, Julia Suh, Dong Sun, Toosi, Mehran Beiraghi, Maroofian, Reza, Schaefer, Gerald Bradley, Russ-Hall, Sophie, Carvill, Gemma L., Mefford, Heather, Acosta, Maria T., Adams, David R., Amendola, Laura, Bademci, Guney, Balasubramanyam, Ashok, Beck, Anita, Bican, Anna, Blue, Elizabeth, Botto, Lorenzo, Boyd, Brenna, Briere, Lauren C., Brown, Gabrielle, Carey, John, Crouse, Andrew B., Dipple, Katrina, Doss, Argenia L., Douine, Emilie D., Eckstein, David J., Fieg, Elizabeth L., Forghani, Irman, Godfrey, Rena A., Grajewski, Alana, Hahn, Sihoun, Hisama, Fuki M., Hutchison, Sarah, Introne, Wendy, Ketkar, Shamika, Kiley, Dana, Kilich, Gonench, Korrick, Susan, Kozuira, Mary, Krakow, Deborah, Kravets, Elijah, Lalani, Seema R., LeBlanc, Kimberly, Levitt, Roy, Lewis, Richard A., Loo, Sandra K., Mahoney, Rachel, Mao, Rong, Maravilla, Kenneth, Marwaha, Shruti, McCray, Alexa T., Mefford, Heather, Merritt, J. Lawrence, Morava, Eva, Nakano-Okuno, Mariko, Nelson, Stanley F., Phillips III, John A., Posey, Jennifer E., Potocki, Lorraine, Rao, Deepak A., Raskind, Wendy, Renteria, Genecee, Reuter, Chloe M., Robertson, Amy K., Rossignol, Francis, Ruzhnikov, Maura, Saporta, Mario, Seto, Elaine, Sisco, Kathy, Spillmann, Rebecca C., Stoler, Joan M., Tabor, Holly K., Tan, Queenie K.-G., Tan, Amelia L.M., Telischi, Fred, Tifft, Cynthia J., Toro, Camilo, Tran, Alyssa A., Ungar, Rachel A., Vogel, Tiphanie P., Wallace, Stephanie, Wambach, Jennifer, Wegner, Daniel, Wener, Mark, Wenger, Tara, Westerfield, Monte, Worley, Kim, Xiao, Changrui, Yang, John, Chao, Hsiao-Tuan

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Endocannabinoid dysfunction in neurological disease: neuro-ocular DAGLA-related syndrome von Bainbridge, Matthew N, Mazumder, Aloran, Ogasawara, Daisuke, Abou Jamra, Rami, Bernard, Geneviève, Bertini, Enrico, Burglen, Lydie, Cope, Heidi, Crawford, Ali, Derksen, Alexa, Dure, Leon, Gantz, Emily, Koch-Hogrebe, Margarete, Hurst, Anna C E, Mahida, Sonal, Marshall, Paige, Micalizzi, Alessia, Novelli, Antonio, Peng, Hongfan, Rodriguez, Diana, Robbins, Shira L, Rutledge, S Lane, Scalise, Roberta, Schließke, Sophia, Shashi, Vandana, Srivastava, Siddharth, Thiffault, Isabella, Topol, Sarah, Qebibo, Leila, Wieczorek, Dagmar, Cravatt, Benjamin, Haricharan, Svasti, Torkamani, Ali, Friedman, Jennifer

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Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder von Schneeberger, Pauline E, Kortüm, Fanny, Korenke, Georg Christoph, Alawi, Malik, Santer, René, Woidy, Mathias, Buhas, Daniela, Fox, Stephanie, Juusola, Jane, Alfadhel, Majid, Webb, Bryn D, Coci, Emanuele G, Abou Jamra, Rami, Siekmeyer, Manuela, Biskup, Saskia, Heller, Corina, Maier, Esther M, Javaher-Haghighi, Poupak, Bedeschi, Maria F, Ajmone, Paola F, Iascone, Maria, Peeters, Hilde, Ballon, Katleen, Jaeken, Jaak, Rodríguez Alonso, Aroa, Palomares-Bralo, María, Santos-Simarro, Fernando, Meuwissen, Marije E C, Beysen, Diane, Kooy, R Frank, Houlden, Henry, Murphy, David, Doosti, Mohammad, Karimiani, Ehsan G, Mojarrad, Majid, Maroofian, Reza, Noskova, Lenka, Kmoch, Stanislav, Honzik, Tomas, Cope, Heidi, Sanchez-Valle, Amarilis, Gelb, Bruce D, Kurth, Ingo, Hempel, Maja, Kutsche, Kerstin

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De novo variants in DENND5B cause a neurodevelopmental disorder von Scala, Marcello, Ferla, Matteo, Fatemi, Ali, Phillips, John A., Rio, Marlene, Siquier, Karine, Musante, Ilaria, Baldassari, Simona, Iacomino, Michele, Acosta, Maria T., Allworth, Aimee, Afzali, Ben, Bademci, Guney, Beck, Anita, Berry, Gerard T., Bican, Anna, Bohnsack, John, Botto, Lorenzo, Brown, Gabrielle, Carrasquillo, Olveen, Chanprasert, Sirisak, Chao, HsiaoTuan, Chinn, Ivan, Clark, Gary D., Cope, Heidi, Craigen, William J., D’Souza, Precilla, Dipple, Katrina, Doherty, Daniel, Doss, Argenia L., Fisher, Paul G., Fogel, Brent L., Gahl, William A., Glass, Ian, Godfrey, Rena A., Grajewski, Alana, Gropman, Andrea, Halley, Meghan C., Hanchard, Neal, Hassey, Kelly, Hayes, Nichole, Hom, Jason, Huang, Alden, Introne, Wendy, Jarvik, Jeffrey, Jobanputra, Vaidehi, Kilich, Gonench, Kohler, Jennefer N., Korrick, Susan, Krasnewich, Donna M., Lam, Byron, Lam, Christina, Lanpher, Brendan C., Loscalzo, Joseph, Maas, Richard L., Macnamara, Ellen F., Maduro, Valerie V., Marth, Gabor, Martin, Beth A., Marwaha, Shruti, McConkie-Rosell, Allyn, McCray, Alexa T., Moretti, Paolo, Morimoto, Marie, Nakano-Okuno, Mariko, Nieves-Rodriguez, Shirley, Orengo, James P., Pace, Laura, Parker, Neil H., Quinlan, Aaron, Raper, Anna, Reuter, Chloe M., Rives, Lynette, Robertson, Amy K., Rodan, Lance H., Rossignol, Francis, Saporta, Mario, Schaechter, Judy, Seto, Elaine, Shelkowitz, Emily, Shin, Jimann, Solnica-Krezel, Lilianna, Sweetser, David A., Sybert, Virginia, Tarakad, Arjun, Velinder, Matt, Viskochil, Dave, Ward, Patricia A., Wegner, Daniel, Weisz Hubshman, Monika, Wener, Mark, Wenger, Tara, Reed, Sara, Al Saif, Hind, Walsh, Matthew B., Gustincich, Stefano, Ruggiero, Sarah M., Fitzgerald, Mark P., Helbig, Ingo, Severino, Mariasavina

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Macrocephaly and developmental delay caused by missense variants in RAB5C von Koop, Klaas, Yuan, Weimin, Tessadori, Federico, Rodriguez-Polanco, Wilmer R, Grubbs, Jeremy, Zhang, Bo, Osmond, Matt, Graham, Gail, Sawyer, Sarah, Conboy, Erin, Vetrini, Francesco, Treat, Kayla, Płoski, Rafal, Pienkowski, Victor Murcia, Kłosowska, Anna, Fieg, Elizabeth, Krier, Joel, Mallebranche, Coralie, Alban, Ziegler, Aldinger, Kimberly A, Ritter, Deborah, Macnamara, Ellen, Sullivan, Bonnie, Herriges, John, Alaimo, Joseph T, Helbig, Catherine, Ellis, Colin A, van Eyk, Clare, Gecz, Jozef, Farrugia, Daniel, Osei-Owusu, Ikeoluwa, Adès, Lesley, van den Boogaard, Marie-Jose, Fuchs, Sabine, Bakker, Jeroen, Duran, Karen, Dawson, Zachary D, Lindsey, Anika, Huang, Huiyan, Baldridge, Dustin, Silverman, Gary A, Grant, Barth D, Raizen, David, van Haaften, Gijs, Pak, Stephen C, Rehmann, Holger, Schedl, Tim, van Hasselt, Peter

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Genomics Research with Undiagnosed Children: Ethical Challenges at the Boundaries of Research and Clinical Care von Maghiro, AudreyStephannie, Tabor, Holly K., Acosta, Maria T., Amendola, Laura, Andrews, Ashley, Balasubramanyam, Ashok, Baldridge, Dustin, Bennett, Jimmy, Berg-Rood, Beverly, Berry, Gerard T., Bican, Anna, Bohnsack, John, Boyd, Brenna, Burke, Elizabeth A., Byers, Peter, Peter Chang, Ta Chen, Chanprasert, Sirisak, Clark, Gary D., Cobban, Laurel A., Cogan, Joy D., Sessions Cole, F., Colley, Heather A., Cope, Heidi, D'Souza, Precilla, Dasari, Surendra, Dipple, Katrina, Doherty, Daniel, Dorrani, Naghmeh, Earl, Dawn, Falk, Marni, Fieg, Elizabeth L., Fisher, Paul G., Gahl, William A., Goddard, Page C., Golden-Grant, Katie, Grajewski, Alana, Hahn, Sihoun, Hamid, Rizwan, Hassey, Kelly, Holm, Ingrid A., Hom, Jason, Introne, Wendy, Izumi, Kosuke, Jayadev, Suman, Kiley, Dana, Kobren, Shilpa N., Korrick, Susan, Krasnewich, Donna M., Lam, Christina, Lanza, Ian R., Lee, Brendan H., Loo, Sandra K., Maas, Richard L., Macnamara, Ellen F., MacRae, Calum A., Manolio, Teri A., Marth, Gabor, McConkie-Rosell, Allyn, Mefford, Heather, Nickerson, Deborah, Nieves-Rodriguez, Shirley, Novacic, Donna, Oglesbee, Devin, Pace, Laura, Posey, Jennifer E., Potocki, Lorraine, Rao, Deepak A., Raskind, Wendy, Renteria, Genecee, Robertson, Amy K., Rossignol, Francis, Ruzhnikov, Maura, Scott, Daryl A., Shashi, Vandana, Shin, Jimann, Sisco, Kathy, Smith, Edward C., Solomon, Ben, Sullivan, Jennifer A., Sybert, Virginia, Tan, Amelia L.M., Tekin, Mustafa, Telischi, Fred, Toro, Camilo, Ungar, Rachel A., Vanderver, Adeline, Walker, Melissa, Walley, Nicole M., Wambach, Jennifer, Wan, Jijun, Wang, Lee-kai, Ward, Patricia A., Wegner, Daniel, Hubshman, Monika Weisz, Wener, Mark, Wenger, Tara, Westerfield, Monte, Worley, Kim, Xiao, Changrui, Yang, John

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Respiratory Outcomes of Infants Born Extremely Preterm in the Necrotizing Enterocolitis Surgery Trial von DeMauro, Sara B., Jensen, Erik A., Tyson, Jon, Keszler, Martin, Kilbride, Howard W., Cahill, Tanya E., Kirker, Kristin, Hayes, Devan, Laughon, Matthew M., Fisher, Kimberley A., Bose, Gennie, Wereszczak, Janice, Kicklighter, Stephen D., Patel, Ravi M., Carlton, David P., Stoll, Barbara J., Maitre, Nathalie L., Loggins, Yvonne, Hale, Ellen C., Bottcher, Diane, Carter, Sheena L., Wineski, Lynn, Dawn Wilson, Leslie, Eason, Elizabeth, Lally, Kevin, Allain, Elizabeth, Arldt-McAlister, Julie, Boricha, Fatima, John, Janice, McDavid, Georgia E., Siddiki, Saba, Sperry, Daniel K., Stephens, Emily, Wright, Sharon L., Nelin, Leif D., Yeates, Keith O., Luzader, Patricia, Hague, Cole D., Sullivan, Margaret, Small, Kristi, Fortney, Christine A., Beckford, Demi R., Levengood, Katelyn, Das, Abhik, Bann, Carla M., Gantz, Marie G., O’Donnell Auman, Jeanette, Crawford, Margaret, Parlberg, Lindsay, Chock, Valerie Y., Earhart, Beth, Proud, Melinda S., MacKinnon, Brenda L., Peralta-Carcelen, Myriam, Biasini, Fred J., Chopko, Stephanie A., McNair, Tara E., Chanlaw, Teresa, Johnson, Karen J., Van Muyden, Sarah, Watterberg, Kristi L., Hartenberger, Carol, Schmidt, Barbara, Kirpalani, Haresh, Cucinotta, Dara M., Hurt, Hallam, Reynolds, Anne Marie, Wadkins, Holly I.M., Scorsone, Ann Marie, Orme, Constance, Li, Emily, Coleman, Kelly R., Stevens, Timothy, Pegoli, Walter, Wynn, Karen, Conway, Patrick, Williams, Ashley, Brion, Luc P., Vasil, Diana M., Chen, Lijun, Lee, Lizette E., Boatman, Cathy Twell, Tolentino-Plata, Kristine, Gerday, Erick B., Rau, Carrie A., Cunningham, Sean D., Hall, Becky, Loertscher, Manndi C., McGrath, Kandace M., Morshedzadeh, Galina, Stout, Kelly, Weaver-Lewis, Kimberlee, Shankaran, Seetha, Pappas, Athina, Chawla, Sanjay, Muran, Gerry, Woldt, Eunice, Goldston, Laura A., Ehrenkranz, Richard A., Poulsen, JoAnn

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De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling von Morleo, Manuela, Briere, Lauren C., Rosello, Marion, Tirozzi, Alfonsina, Tammaro, Roberta, High, Frances A., Adams, David R., Alvey, Justin, Bale, Jim, Bayrak-Toydemir, Pinar, Beggs, Alan H., Behrens, Edward, Bejerano, Gill, Bonner, Devon, Butte, Manish J., Byrd, William E., Cassini, Thomas, Coakley, Terra R., Cobban, Laurel A., Cole, F. Sessions, Colley, Heather A., Dai, Hongzheng, Davis, Joie, Douine, Emilie D., Eckstein, David J., Emrick, Lisa T., Hadley, Don, Hamid, Rizwan, Hassey, Kelly, Hayes, Nichole, Horike-Pyne, Martha, Huang, Alden, Isasi, Rosario, Izumi, Kosuke, Jarvik, Gail P., Jarvik, Jeffrey, Jobanputra, Vaidehi, Karaviti, Lefkothea, Korrick, Susan, Krasnewich, Donna M., Lam, Byron, Liu, Pengfei, Longo, Nicola, Loscalzo, Joseph, Maas, Richard L., Macnamara, Ellen F., Maduro, Valerie V., Manolio, Teri A., Marwaha, Shruti, Mirzaa, Ghayda, Morava, Eva, Nakano-Okuno, Mariko, Nicholas, Sarah K., Pallais, J. Carl, Raskind, Wendy, Rosenwasser, Natalie, Sampson, Jacinda B., Schedl, Timothy, Shashi, Vandana, Smith, Edward C., Sullivan, Jennifer A., Sweetser, David A., Sybert, Virginia, Tekin, Mustafa, Tran, Alyssa A., Ungar, Rachel A., Vanderver, Adeline, Wallace, Stephanie, Walley, Nicole M., Wambach, Jennifer, Wan, Jijun, Wang, Lee-kai, Ward, Patricia A., Wegner, Daniel, Wener, Mark, Wenger, Tara, Westerfield, Monte, Wolfe, Lynne A., Worley, Kim, Xiao, Changrui, Torella, Annalaura, Morleo, Manuela, Spampanato, Carmine, Pinelli, Michele, Massimello, Marta, Leuzzi, Vincenzo, Romano, Corrado, Amenta, Simona, Grandone, Anna, Marini, Carla, Bigoni, Stefania, Trabacca, Antonio, De Rinaldis, Marta, Ferrante, Luigi, Torella, Annalaura, Tenconi, Romano, van Gassen, Koen L.I., Attie-Bitach, Tania, Zollino, Marcella, Sweetser, David A.

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