학술논문
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'학술논문'
에서 검색결과 308건 | 목록
1~20
Academic Journal
Cuccurullo Claudia; Emanuele Cerulli Irelli; Ugga Lorenzo; Riva, Antonella; D'Amico, Alessandra; Cabet, Sara; Lesca, Gaetan; Bilo, Leonilda; Zara, Federico; Iliescu, Catrinel; Barca, Diana; Fung, France; Helbig, Katherine; Ortiz‐Gonzalez, Xilma; Schelhaas, Helenius J.; Willemsen, Marjolein H.; van der Linden, Inge; Canafoglia, Laura; Courage, Carolina; Gommaraschi, Samuele; Gonzalez‐Alegre, Pedro; Bardakjian, Tanya; Syrbe, Steffen; Schuler, Elisabeth; Lemke, Johannes R.; Vari, Stella; Roende, Gitte; Bak, Mads; Huq, Mahbulul; Powis, Zoe; Johannesen, Katrine M.; Hammer, Trine Bjørg; Møller, Rikke S.; Rabin, Rachel; Pappas, John; Zupanc, Mary L.; Zadeh, Neda; Cohen, Julie; Naidu, Sakkubai; Krey, Ilona; Saneto, Russell; Thies, Jenny; Licchetta, Laura; Tinuper, Paolo; Bisulli, Francesca; Minardi, Raffaella; Bayat, Allan; Villeneuve, Nathalie; Molinari, Florence; Salimi Dafsari, Hormos; Moller, Birk; Leundefined; Roux, Marie; Houdayer, Clara; Vecchi, Marilena; Mammi, Isabella; Fiorini, Elena; Proietti, Jacopo; Ferri, Sofia; Cantalupo, Gaetano; Battaglia, Domenica Immacolata; Gambardella, Maria Luigia; Contaldo, Ilaria; Brogna, Claudia; Trivisano, Marina; Deundefined; Dominicis, Angela; Bova, Stefania Maria; Gardella, Elena; Striano, Pasquale; Coppola, Antonietta
Epilepsia, 65, 9, pp. 2728-2750
P271: Two copies, one condition? Understanding APOE allele state in over 14,000 symptomatic patients
Academic Journal
Genetics in Medicine Open. 3
Academic Journal
Bobby G. Ng; Erik A. Eklund; Jill A. Rosenfeld; Abdallah F. Elias; Aya Abu-El-Haija; Celine Bris; Magalie Barth; Jong-Hee Chae; Murim Choi; Holly A. Dubbs; Carl Fratter; Nicola Foulds; Candace Gamble; Ralitza H. Gavrilova; Jaclyn Haven; Trevor L. Hoffman; Jill V. Hunter; Austin Larson; Timothy Edward Lotze; Pilar Magoulas; Emily C. Magness; Debra M. Bootin; Eric D. Marsh; Victoria Nesbitt; Matthew T. Pastore; Joanna Poulton; Shamima Rahman; Fernando Scaglia; Chaya Murali; Jennifer Posey; Joshua Rotenberg; Betsy Schmalz; Deepali N. Shinde; Zöe Powis; Rivka Sukenik-Halevy; Kristen V. Truxal; Tami Uster; Matheus Vernet Machado Bressan Wilke; Erik Klee; Hyewon Woo; Donald Younkin; Jianhua Zhao; Jorge Granadillo; Seema Lalani; David Chitayat; Wendy K. Chung; Hudson H. Freeze; Volkan Okur
Genetics in Medicine Open, Vol 3, Iss , Pp 103425- (2025)
Academic Journal
Palmer, Elizabeth E.; Pusch, Michael; Picollo, Alessandra; Forwood, Caitlin; Nguyen, Matthew H.; Suckow, Vanessa; Gibbons, Jessica; Hoff, Alva; Sigfrid, Lisa; Megarbane, Andre; Nizon, Mathilde; Cogne, Benjamin; Beneteau, Claire; Alkuraya, Fowzan S.; Chedrawi, Aziza; Hashem, Mais O.; Stamberger, Hannah; Weckhuysen, Sarah; Vanlander, Arnaud; Ceulemans, Berten; Rajagopalan, Sulekha; Nunn, Kenneth; Arpin, Stephanie; Raynaud, Martine; Motter, Constance S.; Ward-Melver, Catherine; Janssens, Katrien; Meuwissen, Marije; Beysen, Diane; Dikow, Nicola; Grimmel, Mona; Haack, Tobias B.; Clement, Emma; McTague, Amy; Hunt, David; Townshend, Sharron; Ward, Michelle; Richards, Linda J.; Simons, Cas; Costain, Gregory; Dupuis, Lucie; Mendoza-Londono, Roberto; Dudding-Byth, Tracy; Boyle, Jackie; Saunders, Carol; Fleming, Emily; El Chehadeh, Salima; Spitz, Marie-Aude; Piton, Amelie; Gerard, Benedicte; Warde, Marie-Therese Abi; Rea, Gillian; McKenna, Caoimhe; Douzgou, Sofia; Banka, Siddharth; Akman, Cigdem; Bain, Jennifer M.; Sands, Tristan T.; Wilson, Golder N.; Silvertooth, Erin J.; Miller, Lauren; Lederer, Damien; Sachdev, Rani; Macintosh, Rebecca; Monestier, Olivier; Karadurmus, Deniz; Collins, Felicity; Carter, Melissa; Rohena, Luis; Willemsen, Marjolein H.; Ockeloen, Charlotte W.; Pfundt, Rolph; Kroft, Sanne D.; Field, Michael; Laranjeira, Francisco E. R.; Fortuna, Ana M.; Soares, Ana R.; Michaud, Vincent; Naudion, Sophie; Golla, Sailaja; Weaver, David D.; Bird, Lynne M.; Friedman, Jennifer; Clowes, Virginia; Joss, Shelagh; Polsler, Laura; Campeau, Philippe M.; Blazo, Maria; Bijlsma, Emilia K.; Rosenfeld, Jill A.; Beetz, Christian; Powis, Zoe; McWalter, Kirsty; Brandt, Tracy; Torti, Erin; Mathot, Mikael; Mohammad, Shekeeb S.; Armstrong, Ruth; Kalscheuer, Vera M.
Molecular Psychiatry. 28(2):668-697
Academic Journal
Jessica Lee; Kathleen M Powis; Alejandra Martinez; Jennifer Green; Paige L Williams; Cristina Hernández; Lisa B Haddad; Anna-Barbara Moscicki; Lynn M Yee; Kunjal Patel; Deborah Kacanek; Suzanne Siminski; Mariam Davtyan; Tzy-Jyun Yao; Denise L Jacobson; Tamarra James-Todd; Ellen G Chadwick; Emily A Barr; Claire A Berman; Alex DiPerna; Amanda Flores; Laurie Hyzy; Jennifer Jao; Anisa Khadraoui; Kathleen M Malee; Lisa-Gaye Robinson; Liz Salomon; Kimbrae Sanders; Renee A Smith; Tracy Wolbach; Lela Lartey; Kathleen Malee; Mary Paul; Lynnette Harris; Murli Purswani; Martha Cavallo; Mahoobullah Mirza Baig; Alma Villegas-Schwalenberg; Kierra Archer; Alan Bernegger; Patricia Garvie; Katherine Knapp; Chloe Burkhead; Gheri Terry; Megan Wilkins; Margarita Silio; Dornese Jones; Medea Gabriel; Patricia Sirois; Cecelia Hutto; Paige Hickman; Dan Marullo; Elizabeth McFarland; Carrie Chambers; Robin McEvoy; Mobeen Rathore; Saniyyah Mahmoudi; Staci Routman; Gwendolyn Scott; Lorena Bracho; Anai Cuadra; Zoe M. Rodriguez; Lizmarie Torres; Nydia Scalley; Toniette Frederick; Guadalupe Morales Avendano
BMJ Open, Vol 14, Iss 7 (2024)
Academic Journal
Tessadori, Federico; Duran, Karen; Knapp, Karen; Fellner, Matthias; Deciphering Developmental Disorders Study; Smithson, Sarah; Beleza Meireles, Ana; Elting, Mariet W; Waisfisz, Quinten; O'Donnell-Luria, Anne; Nowak, Catherine; Douglas, Jessica; Ronan, Anne; Brunet, Theresa; Kotzaeridou, Urania; Svihovec, Shayna; Saenz, Margarita S; Thiffault, Isabelle; Del Viso, Florencia; Devine, Patrick; Rego, Shannon; Tenney, Jessica; van Haeringen, Arie; Ruivenkamp, Claudia A L; Koene, Saskia; Robertson, Stephen P; Deshpande, Charulata; Pfundt, Rolph; Verbeek, Nienke; van de Kamp, Jiddeke M; Weiss, Janneke M M; Ruiz, Anna; Gabau, Elisabeth; Banne, Ehud; Pepler, Alexander; Bottani, Armand; Laurent, Sacha; Guipponi, Michel; Bijlsma, Emilia; Bruel, Ange-Line; Sorlin, Arthur; Willis, Mary; Powis, Zoe; Smol, Thomas; Vincent-Delorme, Catherine; Baralle, Diana; Colin, Estelle; Revencu, Nicole; Calpena, Eduardo; Wilkie, Andrew O M; Chopra, Maya; Cormier-Daire, Valerie; Keren, Boris; Afenjar, Alexandra; Niceta, Marcello; Terracciano, Alessandra; Specchio, Nicola; Tartaglia, Marco; Rio, Marlene; Barcia, Giulia; Rondeau, Sophie; Colson, Cindy; Bakkers, Jeroen; Mace, Peter D; Bicknell, Louise S; van Haaften, Gijs
Am J Hum Genet
AMERICAN JOURNAL OF HUMAN GENETICS
r-I3PT. Repositorio Institucional Producción Científica del Institut d'Investigació i Innovació Parc Taulí
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Deciphering Developmental Disorders Study 2022, 'Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome', American journal of human genetics, vol. 109, no. 4, pp. 750-758. https://doi.org/10.1016/j.ajhg.2022.02.003
American Journal of Human Genetics, 109, 4, pp. 750-758
American journal of human genetics, Vol. 109, no. 4, p. 750-758 (2022)
Am. J. Hum. Genet. 109, 750-758 (2022)
AMERICAN JOURNAL OF HUMAN GENETICS
r-I3PT. Repositorio Institucional Producción Científica del Institut d'Investigació i Innovació Parc Taulí
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Deciphering Developmental Disorders Study 2022, 'Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome', American journal of human genetics, vol. 109, no. 4, pp. 750-758. https://doi.org/10.1016/j.ajhg.2022.02.003
American Journal of Human Genetics, 109, 4, pp. 750-758
American journal of human genetics, Vol. 109, no. 4, p. 750-758 (2022)
Am. J. Hum. Genet. 109, 750-758 (2022)
Academic Journal
Genetics in Medicine Open. 2
Academic Journal
Theodore G. Drivas; Dong Li; Divya Nair; Joseph T. Alaimo; Mariëlle Alders; Janine Altmüller; Tahsin Stefan Barakat; E. Martina Bebin; Nicole L. Bertsch; Patrick R. Blackburn; Alyssa Blesson; Arjan M. Bouman; Knut Brockmann; Perrine Brunelle; Margit Burmeister; Gregory M. Cooper; Jonas Denecke; Anne Dieux-Coëslier; Holly Dubbs; Alejandro Ferrer; Danna Gal; Lauren E. Bartik; Lauren B. Gunderson; Linda Hasadsri; Mahim Jain; Catherine Karimov; Beth Keena; Eric W. Klee; Katja Kloth; Baiba Lace; Marina Macchiaiolo; Julien L. Marcadier; Jeff M. Milunsky; Melanie P. Napier; Xilma R. Ortiz-Gonzalez; Pavel N. Pichurin; Jason Pinner; Zoe Powis; Chitra Prasad; Francesca Clementina Radio; Kristen J. Rasmussen; Deborah L. Renaud; Eric T. Rush; Carol Saunders; Duygu Selcen; Ann R. Seman; Deepali N. Shinde; Erica D. Smith; Thomas Smol; Lot Snijders Blok; Joan M. Stoler; Sha Tang; Marco Tartaglia; Michelle L. Thompson; Jiddeke M. van de Kamp; Jingmin Wang; Dagmar Weise; Karin Weiss; Rixa Woitschach; Bernd Wollnik; Huifang Yan; Elaine H. Zackai; Giuseppe Zampino; Philippe Campeau; Elizabeth Bhoj
Eur J Hum Genet
Drivas, T G, Li, D, Nair, D, Alaimo, J T, Alders, M, Altmüller, J, Barakat, T S, Bebin, E M, Bertsch, N L, Blackburn, P R, Blesson, A, Bouman, A M, Brockmann, K, Brunelle, P, Burmeister, M, Cooper, G M, Denecke, J, Dieux-Coëslier, A, Dubbs, H, Ferrer, A, Gal, D, Bartik, L E, Gunderson, L B, Hasadsri, L, Jain, M, Karimov, C, Keena, B, Klee, E W, Kloth, K, Lace, B, Macchiaiolo, M, Marcadier, J L, Milunsky, J M, Napier, M P, Ortiz-Gonzalez, X R, Pichurin, P N, Pinner, J,Powis , Z, Prasad, C, Radio, F C, Rasmussen, K J, Renaud, D L, Rush, E T, Saunders, C, Selcen, D, Seman, A R, Shinde, D N, Smith, E D, Smol, T, Snijders Blok, L, Stoler, J M, Tang, S, Tartaglia, M, Thompson, M L, van de Kamp, J M, Wang, J, Weise, D, Weiss, K, Woitschach, R, Wollnik, B, Yan, H, Zackai, E H, Zampino, G, Campeau, P & Bhoj, E 2020, 'A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome', European Journal of Human Genetics, vol. 28, no. 10, pp. 1422-1431. https://doi.org/10.1038/s41431-020-0654-4
Paediatrics Publications
Drivas, T G, Li, D, Nair, D, Alaimo, J T, Alders, M, Altmüller, J, Barakat, T S, Bebin, E M, Bertsch, N L, Blackburn, P R, Blesson, A, Bouman, A M, Brockmann, K, Brunelle, P, Burmeister, M, Cooper, G M, Denecke, J, Dieux-Coëslier, A, Dubbs, H, Ferrer, A, Gal, D, Bartik, L E, Gunderson, L B, Hasadsri, L, Jain, M, Karimov, C, Keena, B, Klee, E W, Kloth, K, Lace, B, Macchiaiolo, M, Marcadier, J L, Milunsky, J M, Napier, M P, Ortiz-Gonzalez, X R, Pichurin, P N, Pinner, J,
Paediatrics Publications
P271: Beyond SMN1: Review of genotype-phenotype correlation in individuals with ≥4 SMN2 copy numbers
Academic Journal
Genetics in Medicine Open. 1(1)
Academic Journal
Blok, Lot Snijders; Kleefstra, Tjitske; Venselaar, Hanka; Maas, Saskia; Kroes, Hester Y.; Lachmeijer, Augusta M. A.; van Gassen, Koen L., I; Firth, Helen, V; Tomkins, Susan; Bodek, Simon; Study, The D. D. D.; Ounap, Katrin; Wojcik, Monica H.; Cunniff, Christopher; Bergstrom, Katherine; Powis, Zoe; Tang, Sha; Shinde, Deepali N.; Au, Catherine; Iglesias, Alejandro D.; Izumi, Kosuke; Leonard, Jacqueline; Abou Tayoun, Ahmad; Baker, Samuel W.; Tartaglia, Marco; Niceta, Marcello; Dentici, Maria Lisa; Okamoto, Nobuhiko; Miyake, Noriko; Matsumoto, Naomichi; Vitobello, Antonio; Faivre, Laurence; Philippe, Christophe; Gilissen, Christian; Wiel, Laurens; Pfundt, Rolph; Deriziotis, Pelagia; Brunner, Han G.; Fisher, Simon E.
The American Journal of Human Genetics
American Journal of Human Genetics, 105, 2, pp. 403-412
American Journal of Human Genetics, 105, 2, pp. 403-412
Academic Journal
Straub, Jonas; Konrad, Enrico D. H.; Gruner, Johanna; Toutain, Annick; Bok, Levinus A.; Cho, Megan T.; Crawford, Heather P.; Dubbs, Holly; Douglas, Ganka; Jobling, Rebekah; Johnson, Diana; Krock, Bryan; Mikati, Mohamad A.; Nesbitt, Addie; Nicolai, Joost; Phillips, Meredith; Poduri, Annapurna; Ortiz-Gonzalez, Xilma R.; Powis, Zoe; Santani, Avni; Smith, Lacey; Stegmann, Alexander P. A.; Stumpel, Constance; Vreeburg, Maaike; Fliedner, Anna; Gregor, Anne; Sticht, Heinrich; Zweier, Christiane
The American Journal of Human Genetics. 102:44-57
Academic Journal
Zweier, Markus; Begemann, Anaïs; McWalter, Kirsty; Cho, Megan T.; Abela, Lucia; Banka, Siddharth; Behring, Bettina; Berger, Andrea; Brown, Chester W.; Carneiro, Maryline; Chen, Jiani; Cooper, Gregory M.; Deciphering Developmental Disorders (DDD) Study; Finnila, Candice R.; Guillen Sacoto, Maria J.; Henderson, Alex; Hüffmeier, Ulrike; Joset, Pascal; Kerr, Bronwyn; Lesca, Gaetan; Leszinski, Gloria S.; McDermott, John Henry; Meltzer, Meira R.; Monaghan, Kristin G.; Mostafavi, Roya; Õunap, Katrin; Plecko, Barbara; Powis, Zöe; Purcarin, Gabriela; Reimand, Tiia; Riedhammer, Korbinian M.; Schreiber, John M.; Sirsi, Deepa; Wierenga, Klaas J.; Wojcik, Monica H.; Papuc, Sorina M.; Steindl, Katharina; Sticht, Heinrich; Rauch, Anita
European Journal of Human Genetics. 27(5):747-759
Academic Journal
Samin A. Sajan; Zöe Powis; Katherine L. Helbig; Honey Nagakura; Ladonna Immken; Sha Tang; Wendy A. Alcaraz
Clinical Case Reports, Vol 6, Iss 7, Pp 1208-1213 (2018)
Academic Journal
Bryant, Laura; Li, Dong; Sherr, Elliott; Thompson, Michelle L; McWalter, Kirsty; Stumpel, Constance T R M; Stevens, Servi J C; Stegmann, Alexander P A; Tveten, Kristian; Vøllo, Arve; Prescott, Trine; Fagerberg, Christina; Laulund, Lone Walentin; Fregeau, Brieana; Larsen, Martin J; Byler, Melissa; Lebel, Robert Roger; Hurst, Anna C; Dean, Joy; Schrier Vergano, Samantha A; Norman, Jennifer; Mercimek-Andrews, Saadet; Neira, Juanita; Van Allen, Margot I; Wierenga, Klaas J; Longo, Nicola; Sellars, Elizabeth; Louie, Raymond J; Cathey, Sara S; Brokamp, Elly; Heron, Delphine; Snyder, Molly; Vanderver, Adeline; Simon, Celeste; de la Cruz, Xavier; Wadley, Alexandrea; Padilla, Natália; Crump, J Gage; Chung, Wendy; Garcia, Benjamin; Hakonarson, Hakon H; Bhoj, Elizabeth J; Mancini, Grazia M S; Powell-Hamilton, Nina; van de Kamp, Jiddeke; Grebe, Theresa; Dean, John; Ross, Alison; Cox, Samuel G; Crawford, Heather P; Powis, Zoe; Cho, Megan T; Willing, Marcia C; Manwaring, Linda; Schot, Rachel; Nava, Caroline; Afenjar, Alexandra; Lessel, Davor; Wagner, Matias; Marchione, Dylan; Klopstock, Thomas; Winkelmann, Juliane; Catarino, Claudia B; Retterer, Kyle; Schuette, Jane L; Innis, Jeffrey W; Pizzino, Amy; Lüttgen, Sabine; Denecke, Jonas; Strom, Tim M; Joiner, Evan F; Monaghan, Kristin G; Study, DDD; Yuan, Zuo-Fei; Dubbs, Holly; Bend, Renee; Lee, Jennifer A; Lyons, Michael J; Hoefele, Julia; Günthner, Roman; Reutter, Heiko; Wilson, Khadija; Keren, Boris; Radtke, Kelly; Sherbini, Omar; Mrokse, Cameron; Helbig, Katherine L; Odent, Sylvie; Cogne, Benjamin; Mercier, Sandra; Bezieau, Stephane; Besnard, Thomas; Janssen, Kevin; Kury, Sebastien; Redon, Richard; Reinson, Karit; Wojcik, Monica H; Õunap, Katrin; Ilves, Pilvi; Innes, A Micheil; Kernohan, Kristin D; Consortium, Care4Rare Canada; Costain, Gregory; Lee, Pearl; Meyn, M Stephen; Chitayat, David; Zackai, Elaine; Lehman, Anna; Kitson, Hilary; Study, CAUSES; Martin, Martin G; Martinez-Agosto, Julian A; Network, Undiagnosed Diseases; Nelson, Stan F; March, Michael E; Palmer, Christina G S; Papp, Jeanette C; Parker, Neil H; Sinsheimer, Janet S; Vilain, Eric; Wan, Jijun; Yoon, Amanda J; Zheng, Allison; Brimble, Elise; Ferrero, Giovanni Battista; Nair, Divya; Radio, Francesca Clementina; Carli, Diana; Barresi, Sabina; Brusco, Alfredo; Tartaglia, Marco; Thomas, Jennifer Muncy; Umana, Luis; Weiss, Marjan M; Gotway, Garrett; Stuurman, K. E.
Sci Adv
DDD Study, Care4Rare Canada Consortium, CAUSES Study & Undiagnosed Diseases Network 2020, 'Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients', Science Advances, vol. 6, no. 49, eabc9207. https://doi.org/10.1126/sciadv.abc9207
Science advances 6(49), eabc9207 (2020). doi:10.1126/sciadv.abc9207
Bryant, L, Li, D, Cox, S G, Marchione, D, Joiner, E F, Wilson, K, Fagerberg, C, Laulund, L W, Larsen, M J & DDD Study 2020, ' Histone H3.3 beyond cancer : Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients ', Science Advances, vol. 6, no. 49, eabc9207 . https://doi.org/10.1126/sciadv.abc9207
Science advances, vol 6, iss 49
DDD Study, Care4Rare Canada Consortium, CAUSES Study & Undiagnosed Diseases Network 2020, 'Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients', Science Advances, vol. 6, no. 49, eabc9207. https://doi.org/10.1126/sciadv.abc9207
Science advances 6(49), eabc9207 (2020). doi:10.1126/sciadv.abc9207
Bryant, L, Li, D, Cox, S G, Marchione, D, Joiner, E F, Wilson, K, Fagerberg, C, Laulund, L W, Larsen, M J & DDD Study 2020, ' Histone H3.3 beyond cancer : Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients ', Science Advances, vol. 6, no. 49, eabc9207 . https://doi.org/10.1126/sciadv.abc9207
Science advances, vol 6, iss 49
Academic Journal
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-5 (2017)
Academic Journal
Powis, Zöe; Farwell Hagman, Kelly D; Speare, Virginia; Cain, Taylor; Blanco, Kirsten; Mowlavi, Layla S; Mayerhofer, Emily M; Tilstra, David; Vedder, Timothy; Hunter, Jesse M; Tsang, Marilyn; Gonzalez, Lina; Vockley, Gerald; Tang, Sha
Genetics in Medicine: Official journal of the American College of Medical Genetics and Genomics. 20(11):1468-1471
Academic Journal
Zöe Powis; Kelly D. Farwell Hagman; Kirsten Blanco; Margaret Au; John M. Graham; Kathryn Singh; Natalie Gallant; Linda M. Randolph; Meghan Towne; Jesse Hunter; Deepali N. Shinde; Erika Palmaer; Brian Schoenfeld; Sha Tang
Molecular Genetics & Genomic Medicine, Vol 8, Iss 2, Pp n/a-n/a (2020)
Academic Journal
Farwell Hagman, Kelly D; Shinde, Deepali N; Mroske, Cameron; Smith, Erica; Radtke, Kelly; Shahmirzadi, Layla; El-Khechen, Dima; Powis, Zöe; Chao, Elizabeth C; Alcaraz, Wendy A; Helbig, Katherine L; Sajan, Samin A; Rossi, Mari; Lu, Hsiao-Mei; Huether, Robert; Li, Shuwei; Wu, Sitao; Nuñes, Mark E; Tang, Sha
Genetics in Medicine: Official journal of the American College of Medical Genetics and Genomics. 20(9):1099-1102
Academic Journal
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학술DB(Database Provider)
저널명(출판물, Title)
출판사(Publisher)
자료유형(Source Type)
주제어
언어