Results of search for 'au:"Roger, E"' › مکتبة رقمیه للعلوم الطبيه catalog

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	1341.	Dendritic Cells Enhance Polyfunctionality of Adoptively Transferred T Cells That Target Cytomegalovirus in Glioblastoma. [electronic resource] by Reap, Elizabeth A Suryadevara, Carter M Batich, Kristen A Sanchez-Perez, Luis Archer, Gary E Schmittling, Robert J Norberg, Pamela K Herndon, James E Healy, Patrick Congdon, Kendra L Gedeon, Patrick C Campbell, Olivia C Swartz, Adam M Riccione, Katherine A Yi, John S Hossain-Ibrahim, Mohammed K Saraswathula, Anirudh Nair, Smita K Dunn-Pirio, Anastasie M Broome, Taylor M Weinhold, Kent J Desjardins, Annick Vlahovic, Gordana McLendon, Roger E Friedman, Allan H Friedman, Henry S Bigner, Darell D Fecci, Peter E Mitchell, Duane A Sampson, John H Producer: 20181105 In: Cancer research vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1342.	On impact and volcanism across the Cretaceous-Paleogene boundary. [electronic resource] by Hull, Pincelli M Bornemann, André Penman, Donald E Henehan, Michael J Norris, Richard D Wilson, Paul A Blum, Peter Alegret, Laia Batenburg, Sietske J Bown, Paul R Bralower, Timothy J Cournede, Cecile Deutsch, Alexander Donner, Barbara Friedrich, Oliver Jehle, Sofie Kim, Hojung Kroon, Dick Lippert, Peter C Loroch, Dominik Moebius, Iris Moriya, Kazuyoshi Peppe, Daniel J Ravizza, Gregory E Röhl, Ursula Schueth, Jonathan D Sepúlveda, Julio Sexton, Philip F Sibert, Elizabeth C Śliwińska, Kasia K Summons, Roger E Thomas, Ellen Westerhold, Thomas Whiteside, Jessica H Yamaguchi, Tatsuhiko Zachos, James C Producer: 20200519 In: Science (New York, N.Y.) vol. 367 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1343.	A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism. [electronic resource] by Celestino-Soper, Patrícia B S Violante, Sara Crawford, Emily L Luo, Rui Lionel, Anath C Delaby, Elsa Cai, Guiqing Sadikovic, Bekim Lee, Kwanghyuk Lo, Charlene Gao, Kun Person, Richard E Moss, Timothy J German, Jennifer R Huang, Ni Shinawi, Marwan Treadwell-Deering, Diane Szatmari, Peter Roberts, Wendy Fernandez, Bridget Schroer, Richard J Stevenson, Roger E Buxbaum, Joseph D Betancur, Catalina Scherer, Stephen W Sanders, Stephan J Geschwind, Daniel H Sutcliffe, James S Hurles, Matthew E Wanders, Ronald J A Shaw, Chad A Leal, Suzanne M Cook, Edwin H Goin-Kochel, Robin P Vaz, Frédéric M Beaudet, Arthur L Producer: 20120802 In: Proceedings of the National Academy of Sciences of the United States of America vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1344.	TERT promoter mutations occur frequently in gliomas and a subset of tumors derived from cells with low rates of self-renewal. [electronic resource] by Killela, Patrick J Reitman, Zachary J Jiao, Yuchen Bettegowda, Chetan Agrawal, Nishant Diaz, Luis A Friedman, Allan H Friedman, Henry Gallia, Gary L Giovanella, Beppino C Grollman, Arthur P He, Tong-Chuan He, Yiping Hruban, Ralph H Jallo, George I Mandahl, Nils Meeker, Alan K Mertens, Fredrik Netto, George J Rasheed, B Ahmed Riggins, Gregory J Rosenquist, Thomas A Schiffman, Mark Shih, Ie-Ming Theodorescu, Dan Torbenson, Michael S Velculescu, Victor E Wang, Tian-Li Wentzensen, Nicolas Wood, Laura D Zhang, Ming McLendon, Roger E Bigner, Darell D Kinzler, Kenneth W Vogelstein, Bert Papadopoulos, Nickolas Yan, Hai Producer: 20130712 In: Proceedings of the National Academy of Sciences of the United States of America vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1345.	De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies. [electronic resource] by Homsy, Jason Zaidi, Samir Shen, Yufeng Ware, James S Samocha, Kaitlin E Karczewski, Konrad J DePalma, Steven R McKean, David Wakimoto, Hiroko Gorham, Josh Jin, Sheng Chih Deanfield, John Giardini, Alessandro Porter, George A Kim, Richard Bilguvar, Kaya López-Giráldez, Francesc Tikhonova, Irina Mane, Shrikant Romano-Adesman, Angela Qi, Hongjian Vardarajan, Badri Ma, Lijiang Daly, Mark Roberts, Amy E Russell, Mark W Mital, Seema Newburger, Jane W Gaynor, J William Breitbart, Roger E Iossifov, Ivan Ronemus, Michael Sanders, Stephan J Kaltman, Jonathan R Seidman, Jonathan G Brueckner, Martina Gelb, Bruce D Goldmuntz, Elizabeth Lifton, Richard P Seidman, Christine E Chung, Wendy K Producer: 20160202 In: Science (New York, N.Y.) vol. 350 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1346.	Minimum information specification for in situ hybridization and immunohistochemistry experiments (MISFISHIE). [electronic resource] by Deutsch, Eric W Ball, Catherine A Berman, Jules J Bova, G Steven Brazma, Alvis Bumgarner, Roger E Campbell, David Causton, Helen C Christiansen, Jeffrey H Daian, Fabrice Dauga, Delphine Davidson, Duncan R Gimenez, Gregory Goo, Young Ah Grimmond, Sean Henrich, Thorsten Herrmann, Bernhard G Johnson, Michael H Korb, Martin Mills, Jason C Oudes, Asa J Parkinson, Helen E Pascal, Laura E Pollet, Nicolas Quackenbush, John Ramialison, Mirana Ringwald, Martin Salgado, David Sansone, Susanna-Assunta Sherlock, Gavin Stoeckert, Christian J Swedlow, Jason Taylor, Ronald C Walashek, Laura Warford, Anthony Wilkinson, David G Zhou, Yi Zon, Leonard I Liu, Alvin Y True, Lawrence D Producer: 20080709 In: Nature biotechnology vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1347.	Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation. [electronic resource] by Tarpey, Patrick S Stevens, Claire Teague, Jon Edkins, Sarah O'Meara, Sarah Avis, Tim Barthorpe, Syd Buck, Gemma Butler, Adam Cole, Jennifer Dicks, Ed Gray, Kristian Halliday, Kelly Harrison, Rachel Hills, Katy Hinton, Jonathon Jones, David Menzies, Andrew Mironenko, Tatiana Perry, Janet Raine, Keiran Richardson, David Shepherd, Rebecca Small, Alexandra Tofts, Calli Varian, Jennifer West, Sofie Widaa, Sara Yates, Andy Catford, Rachael Butler, Julia Mallya, Uma Moon, Jenny Luo, Ying Dorkins, Huw Thompson, Deborah Easton, Douglas F Wooster, Richard Bobrow, Martin Carpenter, Nancy Simensen, Richard J Schwartz, Charles E Stevenson, Roger E Turner, Gillian Partington, Michael Gecz, Jozef Stratton, Michael R Futreal, P Andrew Raymond, F Lucy Producer: 20070206 In: American journal of human genetics vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1348.	Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor. [electronic resource] by Tarpey, Patrick S Raymond, F Lucy O'Meara, Sarah Edkins, Sarah Teague, Jon Butler, Adam Dicks, Ed Stevens, Claire Tofts, Calli Avis, Tim Barthorpe, Syd Buck, Gemma Cole, Jennifer Gray, Kristian Halliday, Kelly Harrison, Rachel Hills, Katy Jenkinson, Andrew Jones, David Menzies, Andrew Mironenko, Tatiana Perry, Janet Raine, Keiran Richardson, David Shepherd, Rebecca Small, Alexandra Varian, Jennifer West, Sofie Widaa, Sara Mallya, Uma Moon, Jenny Luo, Ying Holder, Susan Smithson, Sarah F Hurst, Jane A Clayton-Smith, Jill Kerr, Bronwyn Boyle, Jackie Shaw, Marie Vandeleur, Lucianne Rodriguez, Jayson Slaugh, Rachel Easton, Douglas F Wooster, Richard Bobrow, Martin Srivastava, Anand K Stevenson, Roger E Schwartz, Charles E Turner, Gillian Gecz, Jozef Futreal, P Andrew Stratton, Michael R Partington, Michael Producer: 20070313 In: American journal of human genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1349.	Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation. [electronic resource] by Tarpey, Patrick S Raymond, F Lucy Nguyen, Lam S Rodriguez, Jayson Hackett, Anna Vandeleur, Lucianne Smith, Raffaella Shoubridge, Cheryl Edkins, Sarah Stevens, Claire O'Meara, Sarah Tofts, Calli Barthorpe, Syd Buck, Gemma Cole, Jennifer Halliday, Kelly Hills, Katy Jones, David Mironenko, Tatiana Perry, Janet Varian, Jennifer West, Sofie Widaa, Sara Teague, John Dicks, Ed Butler, Adam Menzies, Andrew Richardson, David Jenkinson, Andrew Shepherd, Rebecca Raine, Keiran Moon, Jenny Luo, Yin Parnau, Josep Bhat, Shambhu S Gardner, Alison Corbett, Mark Brooks, Doug Thomas, Paul Parkinson-Lawrence, Emma Porteous, Mary E Warner, John P Sanderson, Tracy Pearson, Pauline Simensen, Richard J Skinner, Cindy Hoganson, George Superneau, Duane Wooster, Richard Bobrow, Martin Turner, Gillian Stevenson, Roger E Schwartz, Charles E Futreal, P Andrew Srivastava, Anand K Stratton, Michael R Gécz, Jozef Producer: 20071127 In: Nature genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1350.	De novo mutations in histone-modifying genes in congenital heart disease. [electronic resource] by Zaidi, Samir Choi, Murim Wakimoto, Hiroko Ma, Lijiang Jiang, Jianming Overton, John D Romano-Adesman, Angela Bjornson, Robert D Breitbart, Roger E Brown, Kerry K Carriero, Nicholas J Cheung, Yee Him Deanfield, John DePalma, Steve Fakhro, Khalid A Glessner, Joseph Hakonarson, Hakon Italia, Michael J Kaltman, Jonathan R Kaski, Juan Kim, Richard Kline, Jennie K Lee, Teresa Leipzig, Jeremy Lopez, Alexander Mane, Shrikant M Mitchell, Laura E Newburger, Jane W Parfenov, Michael Pe'er, Itsik Porter, George Roberts, Amy E Sachidanandam, Ravi Sanders, Stephan J Seiden, Howard S State, Mathew W Subramanian, Sailakshmi Tikhonova, Irina R Wang, Wei Warburton, Dorothy White, Peter S Williams, Ismee A Zhao, Hongyu Seidman, Jonathan G Brueckner, Martina Chung, Wendy K Gelb, Bruce D Goldmuntz, Elizabeth Seidman, Christine E Lifton, Richard P Producer: 20130627 In: Nature vol. 498 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1351.	Assembling the brain trust: the multidisciplinary imperative in neuro-oncology. [electronic resource] by Ludmir, Ethan B Mahajan, Anita Ahern, Verity Ajithkumar, Thankamma Alapetite, Claire Bernier-Chastagner, Valérie Bindra, Ranjit S Bishop, Andrew J Bolle, Stephanie Brown, Paul D Carrie, Christian Chalmers, Anthony J Chang, Eric L Chung, Caroline Dieckmann, Karin Esiashvili, Natia Gandola, Lorenza Ghia, Amol J Gondi, Vinai Grosshans, David R Harrabi, Semi B Horan, Gail Indelicato, Danny J Jalali, Rakesh Janssens, Geert O Krause, Mechthild Laack, Nadia N Laperriere, Normand Laprie, Anne Li, Jing Marcus, Karen J McGovern, Susan L Merchant, Thomas E Merrell, Kenneth W Padovani, Laetitia Parkes, Jeannette Paulino, Arnold C Schwarz, Rudolf Shih, Helen A Souhami, Luis Sulman, Erik P Taylor, Roger E Thorp, Nicola Timmermann, Beate Wheeler, Greg Wolden, Suzanne L Woodhouse, Kristina D Yeboa, Debra N Yock, Torunn I Kortmann, Rolf-Dieter McAleer, Mary Frances Producer: 20191128 In: Nature reviews. Clinical oncology vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1352.	Cornelia de Lange syndrome in diverse populations. [electronic resource] by Dowsett, Leah Porras, Antonio R Kruszka, Paul Davis, Brandon Hu, Tommy Honey, Engela Badoe, Eben Thong, Meow-Keong Leon, Eyby Girisha, Katta M Shukla, Anju Nayak, Shalini S Shotelersuk, Vorasuk Megarbane, Andre Phadke, Shubha Sirisena, Nirmala D Dissanayake, Vajira H W Ferreira, Carlos R Kisling, Monisha S Tanpaiboon, Pranoot Uwineza, Annette Mutesa, Leon Tekendo-Ngongang, Cedrik Wonkam, Ambroise Fieggen, Karen Batista, Leticia Cassimiro Moretti-Ferreira, Danilo Stevenson, Roger E Prijoles, Eloise J Everman, David Clarkson, Kate Worthington, Jessica Kimonis, Virginia Hisama, Fuki Crowe, Carol Wong, Paul Johnson, Kisha Clark, Robin D Bird, Lynne Masser-Frye, Diane McDonald, Marie Willems, Patrick Roeder, Elizabeth Saitta, Sulgana Anyane-Yeoba, Kwame Demmer, Laurie Hamajima, Naoki Stark, Zornitza Gillies, Greta Hudgins, Louanne Dave, Usha Shalev, Stavit Siu, Victoria Ades, Ann Dubbs, Holly Raible, Sarah Kaur, Maninder Salzano, Emanuela Jackson, Laird Deardorff, Matthew Kline, Antonie Summar, Marshall Muenke, Maximilian Linguraru, Marius George Krantz, Ian D Producer: 20200206 In: American journal of medical genetics. Part A vol. 179 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1353.	Heterogeneity within the PF-EPN-B ependymoma subgroup. [electronic resource] by Cavalli, Florence M G Hübner, Jens-Martin Sharma, Tanvi Luu, Betty Sill, Martin Zapotocky, Michal Mack, Stephen C Witt, Hendrik Lin, Tong Shih, David J H Ho, Ben Santi, Mariarita Emery, Lyndsey Hukin, Juliette Dunham, Christopher McLendon, Roger E Lipp, Eric S Gururangan, Sridharan Grossbach, Andrew French, Pim Kros, Johan M van Veelen, Marie-Lise C Rao, Amulya A Nageswara Giannini, Caterina Leary, Sarah Jung, Shin Faria, Claudia C Mora, Jaume Schüller, Ulrich Alonso, Marta M Chan, Jennifer A Klekner, Almos Chambless, Lola B Hwang, Eugene I Massimino, Maura Eberhart, Charles G Karajannis, Matthias A Lu, Benjamin Liau, Linda M Zollo, Massimo Ferrucci, Veronica Carlotti, Carlos Tirapelli, Daniela P C Tabori, Uri Bouffet, Eric Ryzhova, Marina Ellison, David W Merchant, Thomas E Gilbert, Mark R Armstrong, Terri S Korshunov, Andrey Pfister, Stefan M Taylor, Michael D Aldape, Kenneth Pajtler, Kristian W Kool, Marcel Ramaswamy, Vijay Producer: 20191008 In: Acta neuropathologica vol. 136 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1354.	Noonan syndrome in diverse populations. [electronic resource] by Kruszka, Paul Porras, Antonio R Addissie, Yonit A Moresco, Angélica Medrano, Sofia Mok, Gary T K Leung, Gordon K C Tekendo-Ngongang, Cedrik Uwineza, Annette Thong, Meow-Keong Muthukumarasamy, Premala Honey, Engela Ekure, Ekanem N Sokunbi, Ogochukwu J Kalu, Nnenna Jones, Kelly L Kaplan, Julie D Abdul-Rahman, Omar A Vincent, Lisa M Love, Amber Belhassan, Khadija Ouldim, Karim El Bouchikhi, Ihssane Shukla, Anju Girisha, Katta M Patil, Siddaramappa J Sirisena, Nirmala D Dissanayake, Vajira H W Paththinige, C Sampath Mishra, Rupesh Klein-Zighelboim, Eva Gallardo Jugo, Bertha E Chávez Pastor, Miguel Abarca-Barriga, Hugo H Skinner, Steven A Prijoles, Eloise J Badoe, Eben Gill, Ashleigh D Shotelersuk, Vorasuk Smpokou, Patroula Kisling, Monisha S Ferreira, Carlos R Mutesa, Leon Megarbane, Andre Kline, Antonie D Kimball, Amy Okello, Emmy Lwabi, Peter Aliku, Twalib Tenywa, Emmanuel Boonchooduang, Nonglak Tanpaiboon, Pranoot Richieri-Costa, Antonio Wonkam, Ambroise Chung, Brian H Y Stevenson, Roger E Summar, Marshall Mandal, Kausik Phadke, Shubha R Obregon, María G Linguraru, Marius G Muenke, Maximilian Producer: 20171130 In: American journal of medical genetics. Part A vol. 173 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1355.	Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders. [electronic resource] by Aref-Eshghi, Erfan Kerkhof, Jennifer Pedro, Victor P Barat-Houari, Mouna Ruiz-Pallares, Nathalie Andrau, Jean-Christophe Lacombe, Didier Van-Gils, Julien Fergelot, Patricia Dubourg, Christèle Cormier-Daire, Valerie Rondeau, Sophie Lecoquierre, François Saugier-Veber, Pascale Nicolas, Gaël Lesca, Gaetan Chatron, Nicolas Sanlaville, Damien Vitobello, Antonio Faivre, Laurence Thauvin-Robinet, Christel Laumonnier, Frederic Raynaud, Martine Alders, Mariëlle Mannens, Marcel Henneman, Peter Hennekam, Raoul C Velasco, Guillaume Francastel, Claire Ulveling, Damien Ciolfi, Andrea Pizzi, Simone Tartaglia, Marco Heide, Solveig Héron, Delphine Mignot, Cyril Keren, Boris Whalen, Sandra Afenjar, Alexandra Bienvenu, Thierry Campeau, Philippe M Rousseau, Justine Levy, Michael A Brick, Lauren Kozenko, Mariya Balci, Tugce B Siu, Victoria Mok Stuart, Alan Kadour, Mike Masters, Jennifer Takano, Kyoko Kleefstra, Tjitske de Leeuw, Nicole Field, Michael Shaw, Marie Gecz, Jozef Ainsworth, Peter J Lin, Hanxin Rodenhiser, David I Friez, Michael J Tedder, Matt Lee, Jennifer A DuPont, Barbara R Stevenson, Roger E Skinner, Steven A Schwartz, Charles E Genevieve, David Sadikovic, Bekim Producer: 20200505 In: American journal of human genetics vol. 106 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1356.	Standardizing global gene expression analysis between laboratories and across platforms. [electronic resource] by Bammler, Theodore Beyer, Richard P Bhattacharya, Sanchita Boorman, Gary A Boyles, Abee Bradford, Blair U Bumgarner, Roger E Bushel, Pierre R Chaturvedi, Kabir Choi, Dongseok Cunningham, Michael L Deng, Shibing Dressman, Holly K Fannin, Rickie D Farin, Fredrico M Freedman, Jonathan H Fry, Rebecca C Harper, Angel Humble, Michael C Hurban, Patrick Kavanagh, Terrance J Kaufmann, William K Kerr, Kathleen F Jing, Li Lapidus, Jodi A Lasarev, Michael R Li, Jianying Li, Yi-Ju Lobenhofer, Edward K Lu, Xinfang Malek, Renae L Milton, Sean Nagalla, Srinivasa R O'malley, Jean P Palmer, Valerie S Pattee, Patrick Paules, Richard S Perou, Charles M Phillips, Ken Qin, Li-Xuan Qiu, Yang Quigley, Sean D Rodland, Matthew Rusyn, Ivan Samson, Leona D Schwartz, David A Shi, Yan Shin, Jung-Lim Sieber, Stella O Slifer, Susan Speer, Marcy C Spencer, Peter S Sproles, Dean I Swenberg, James A Suk, William A Sullivan, Robert C Tian, Ru Tennant, Raymond W Todd, Signe A Tucker, Charles J Van Houten, Bennett Weis, Brenda K Xuan, Shirley Zarbl, Helmut Producer: 20050516 In: Nature methods vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1357.	A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. [electronic resource] by Tarpey, Patrick S Smith, Raffaella Pleasance, Erin Whibley, Annabel Edkins, Sarah Hardy, Claire O'Meara, Sarah Latimer, Calli Dicks, Ed Menzies, Andrew Stephens, Phil Blow, Matt Greenman, Chris Xue, Yali Tyler-Smith, Chris Thompson, Deborah Gray, Kristian Andrews, Jenny Barthorpe, Syd Buck, Gemma Cole, Jennifer Dunmore, Rebecca Jones, David Maddison, Mark Mironenko, Tatiana Turner, Rachel Turrell, Kelly Varian, Jennifer West, Sofie Widaa, Sara Wray, Paul Teague, Jon Butler, Adam Jenkinson, Andrew Jia, Mingming Richardson, David Shepherd, Rebecca Wooster, Richard Tejada, M Isabel Martinez, Francisco Carvill, Gemma Goliath, Rene de Brouwer, Arjan P M van Bokhoven, Hans Van Esch, Hilde Chelly, Jamel Raynaud, Martine Ropers, Hans-Hilger Abidi, Fatima E Srivastava, Anand K Cox, James Luo, Ying Mallya, Uma Moon, Jenny Parnau, Josef Mohammed, Shehla Tolmie, John L Shoubridge, Cheryl Corbett, Mark Gardner, Alison Haan, Eric Rujirabanjerd, Sinitdhorn Shaw, Marie Vandeleur, Lucianne Fullston, Tod Easton, Douglas F Boyle, Jackie Partington, Michael Hackett, Anna Field, Michael Skinner, Cindy Stevenson, Roger E Bobrow, Martin Turner, Gillian Schwartz, Charles E Gecz, Jozef Raymond, F Lucy Futreal, P Andrew Stratton, Michael R Producer: 20090629 In: Nature genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1358.	Williams-Beuren syndrome in diverse populations. [electronic resource] by Kruszka, Paul Porras, Antonio R de Souza, Deise Helena Moresco, Angélica Huckstadt, Victoria Gill, Ashleigh D Boyle, Alec P Hu, Tommy Addissie, Yonit A Mok, Gary T K Tekendo-Ngongang, Cedrik Fieggen, Karen Prijoles, Eloise J Tanpaiboon, Pranoot Honey, Engela Luk, Ho-Ming Lo, Ivan F M Thong, Meow-Keong Muthukumarasamy, Premala Jones, Kelly L Belhassan, Khadija Ouldim, Karim El Bouchikhi, Ihssane Bouguenouch, Laila Shukla, Anju Girisha, Katta M Sirisena, Nirmala D Dissanayake, Vajira H W Paththinige, C Sampath Mishra, Rupesh Kisling, Monisha S Ferreira, Carlos R de Herreros, María Beatriz Lee, Ni-Chung Jamuar, Saumya S Lai, Angeline Tan, Ee Shien Ying Lim, Jiin Wen-Min, Cham Breana Gupta, Neerja Lotz-Esquivel, Stephanie Badilla-Porras, Ramsés Hussen, Dalia Farouk El Ruby, Mona O Ashaat, Engy A Patil, Siddaramappa J Dowsett, Leah Eaton, Alison Innes, A Micheil Shotelersuk, Vorasuk Badoe, Ëben Wonkam, Ambroise Obregon, María Gabriela Chung, Brian H Y Trubnykova, Milana La Serna, Jorge Gallardo Jugo, Bertha Elena Chávez Pastor, Miguel Abarca Barriga, Hugo Hernán Megarbane, Andre Kozel, Beth A van Haelst, Mieke M Stevenson, Roger E Summar, Marshall Adeyemo, A Adebowale Morris, Colleen A Moretti-Ferreira, Danilo Linguraru, Marius George Muenke, Maximilian Producer: 20190520 In: American journal of medical genetics. Part A vol. 176 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1359.	The genome of the domesticated apple (Malus × domestica Borkh.). [electronic resource] by Velasco, Riccardo Zharkikh, Andrey Affourtit, Jason Dhingra, Amit Cestaro, Alessandro Kalyanaraman, Ananth Fontana, Paolo Bhatnagar, Satish K Troggio, Michela Pruss, Dmitry Salvi, Silvio Pindo, Massimo Baldi, Paolo Castelletti, Sara Cavaiuolo, Marina Coppola, Giuseppina Costa, Fabrizio Cova, Valentina Dal Ri, Antonio Goremykin, Vadim Komjanc, Matteo Longhi, Sara Magnago, Pierluigi Malacarne, Giulia Malnoy, Mickael Micheletti, Diego Moretto, Marco Perazzolli, Michele Si-Ammour, Azeddine Vezzulli, Silvia Zini, Elena Eldredge, Glenn Fitzgerald, Lisa M Gutin, Natalia Lanchbury, Jerry Macalma, Teresita Mitchell, Jeff T Reid, Julia Wardell, Bryan Kodira, Chinnappa Chen, Zhoutao Desany, Brian Niazi, Faheem Palmer, Melinda Koepke, Tyson Jiwan, Derick Schaeffer, Scott Krishnan, Vandhana Wu, Changjun Chu, Vu T King, Stephen T Vick, Jessica Tao, Quanzhou Mraz, Amy Stormo, Aimee Stormo, Keith Bogden, Robert Ederle, Davide Stella, Alessandra Vecchietti, Alberto Kater, Martin M Masiero, Simona Lasserre, Pauline Lespinasse, Yves Allan, Andrew C Bus, Vincent Chagné, David Crowhurst, Ross N Gleave, Andrew P Lavezzo, Enrico Fawcett, Jeffrey A Proost, Sebastian Rouzé, Pierre Sterck, Lieven Toppo, Stefano Lazzari, Barbara Hellens, Roger P Durel, Charles-Eric Gutin, Alexander Bumgarner, Roger E Gardiner, Susan E Skolnick, Mark Egholm, Michael Van de Peer, Yves Salamini, Francesco Viola, Roberto Producer: 20101028 In: Nature genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1360.	Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes. [electronic resource] by Mefford, Heather C Sharp, Andrew J Baker, Carl Itsara, Andy Jiang, Zhaoshi Buysse, Karen Huang, Shuwen Maloney, Viv K Crolla, John A Baralle, Diana Collins, Amanda Mercer, Catherine Norga, Koen de Ravel, Thomy Devriendt, Koen Bongers, Ernie M H F de Leeuw, Nicole Reardon, William Gimelli, Stefania Bena, Frederique Hennekam, Raoul C Male, Alison Gaunt, Lorraine Clayton-Smith, Jill Simonic, Ingrid Park, Soo Mi Mehta, Sarju G Nik-Zainal, Serena Woods, C Geoffrey Firth, Helen V Parkin, Georgina Fichera, Marco Reitano, Santina Lo Giudice, Mariangela Li, Kelly E Casuga, Iris Broomer, Adam Conrad, Bernard Schwerzmann, Markus Räber, Lorenz Gallati, Sabina Striano, Pasquale Coppola, Antonietta Tolmie, John L Tobias, Edward S Lilley, Chris Armengol, Lluis Spysschaert, Yves Verloo, Patrick De Coene, Anja Goossens, Linde Mortier, Geert Speleman, Frank van Binsbergen, Ellen Nelen, Marcel R Hochstenbach, Ron Poot, Martin Gallagher, Louise Gill, Michael McClellan, Jon King, Mary-Claire Regan, Regina Skinner, Cindy Stevenson, Roger E Antonarakis, Stylianos E Chen, Caifu Estivill, Xavier Menten, Björn Gimelli, Giorgio Gribble, Susan Schwartz, Stuart Sutcliffe, James S Walsh, Tom Knight, Samantha J L Sebat, Jonathan Romano, Corrado Schwartz, Charles E Veltman, Joris A de Vries, Bert B A Vermeesch, Joris R Barber, John C K Willatt, Lionel Tassabehji, May Eichler, Evan E Producer: 20081023 In: The New England journal of medicine vol. 359 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes. [electronic resource] by

Mefford, Heather C
Sharp, Andrew J
Baker, Carl
Itsara, Andy
Jiang, Zhaoshi
Buysse, Karen
Huang, Shuwen
Maloney, Viv K
Crolla, John A
Baralle, Diana
Collins, Amanda
Mercer, Catherine
Norga, Koen
de Ravel, Thomy
Devriendt, Koen
Bongers, Ernie M H F
de Leeuw, Nicole
Reardon, William
Gimelli, Stefania
Bena, Frederique
Hennekam, Raoul C
Male, Alison
Gaunt, Lorraine
Clayton-Smith, Jill
Simonic, Ingrid
Park, Soo Mi
Mehta, Sarju G
Nik-Zainal, Serena
Woods, C Geoffrey
Firth, Helen V
Parkin, Georgina
Fichera, Marco
Reitano, Santina
Lo Giudice, Mariangela
Li, Kelly E
Casuga, Iris
Broomer, Adam
Conrad, Bernard
Schwerzmann, Markus
Räber, Lorenz
Gallati, Sabina
Striano, Pasquale
Coppola, Antonietta
Tolmie, John L
Tobias, Edward S
Lilley, Chris
Armengol, Lluis
Spysschaert, Yves
Verloo, Patrick
De Coene, Anja
Goossens, Linde
Mortier, Geert
Speleman, Frank
van Binsbergen, Ellen
Nelen, Marcel R
Hochstenbach, Ron
Poot, Martin
Gallagher, Louise
Gill, Michael
McClellan, Jon
King, Mary-Claire
Regan, Regina
Skinner, Cindy
Stevenson, Roger E
Antonarakis, Stylianos E
Chen, Caifu
Estivill, Xavier
Menten, Björn
Gimelli, Giorgio
Gribble, Susan
Schwartz, Stuart
Sutcliffe, James S
Walsh, Tom
Knight, Samantha J L
Sebat, Jonathan
Romano, Corrado
Schwartz, Charles E
Veltman, Joris A
de Vries, Bert B A
Vermeesch, Joris R
Barber, John C K
Willatt, Lionel
Tassabehji, May
Eichler, Evan E

Producer: 20081023 In: The New England journal of medicine vol. 359

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