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1دورية أكاديمية
المؤلفون: Ozcelik, Firat, Dundar, Mehmet Sait, Yildirim, A. Baki, Henehan, Gary, Vicente, Oscar, Sánchez-Alcázar, José A., Gokce, Nuriye, Yildirim, Duygu T., Bingol, Nurdeniz Nalbant, Karanfilska, Dijana Plaseska, Bertelli, Matteo, Pojskic, Lejla, Ercan, Mehmet, Kellermayer, Miklos, Sahin, Izem Olcay, Greiner-Tollersrud, Ole K., Tan, Busra, Martin, Donald, Marks, Robert, Prakash, Satya, Yakubi, Mustafa, Beccari, Tommaso, Lal, Ratnesh, Temel, Sehime G.Aff6, Aff17, Aff18, Fournier, Isabelle, Ergoren, M. Cerkez, Mechler, Adam, Salzet, Michel, Maffia, Michele, Danalev, Dancho, Sun, Qun, Nei, Lembit, Matulis, Daumantas, Tapaloaga, Dana, Janecke, AndresAff28, Aff29, Bown, James, Cruz, Karla Santa, Radecka, Iza, Ozturk, Celal, Nalbantoglu, Ozkan Ufuk, Sag, Sebnem Ozemri, Ko, Kisung, Arngrimsson, Reynir, Belo, Isabel, Akalin, HilalAff1, IDs10142024014179_cor45, Dundar, MunisAff1, IDs10142024014179_cor46
المصدر: Functional & Integrative Genomics. 24(4)
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2دورية أكاديمية
المؤلفون: Ma, Mengqi, Ganapathi, Mythily, Zheng, Yiming, Tan, Kai-Li, Kanca, Oguz, Bove, Kevin E., Quintanilla, Norma, Sag, Sebnem O., Temel, Sehime G., LeDuc, Charles A., McPartland, Amanda J., Pereira, Elaine M., Shen, Yufeng, Hagen, Jacob, Thomas, Christie P., Nguyen Galván, Nhu Thao, Pan, Xueyang, Lu, Shenzhao, Rosenfeld, Jill A., Calame, Daniel G., Wangler, Michael F., Lupski, James R., Pehlivan, Davut, Hertel, Paula M., Chung, Wendy K., Bellen, Hugo J.
المصدر: In Genetics in Medicine July 2024 26(7)
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3
المؤلفون: Fellmann, Florence, van El, Carla G., Charron, Philippe, Michaud, Katarzyna, Howard, Heidi C., Boers, Sarah N., Clarke, Angus J., Duguet, Anne-Marie, Forzano, Francesca, Kauferstein, Silke, Kayserili, Hulya, Lucassen, Anneke, Mendes, Alvaro, Patch, Christine, Radojkovic, Dragica, Rial-Sebbag, Emmanuelle, Sheppard, Mary N., Tasse, Anne-Marie, Temel, Sehime G., Sajantila, Antti, Basso, Cristina, Wilde, Arthur A. M., Cornel, Martina C., Benjamin, Caroline, Borry, Pascal, Clarke, Angus, Cordier, Christophe, Cornel, Martina, van El, Carla, Howard, Heidi, Melegh, Bela, Perola, Markus, Peterlin, Borut, Rogowski, Wolf, Soller, Maria, Stefansdottir, Vigdis, de Wert, Guido
المصدر: European Journal of Human Genetics. 27(12):1763-1773
وصف الملف: electronic
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4دورية أكاديمية
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5دورية أكاديمية
المؤلفون: McMillin, Margaret J, Beck, Anita E, Chong, Jessica X, Shively, Kathryn M, Buckingham, Kati J, Gildersleeve, Heidi IS, Aracena, Mariana I, Aylsworth, Arthur S, Bitoun, Pierre, Carey, John C, Clericuzio, Carol L, Crow, Yanick J, Curry, Cynthia J, Devriendt, Koenraad, Everman, David B, Fryer, Alan, Gibson, Kate, Uzielli, Maria Luisa Giovannucci, Graham, John M, Hall, Judith G, Hecht, Jacqueline T, Heidenreich, Randall A, Hurst, Jane A, Irani, Sarosh, Krapels, Ingrid PC, Leroy, Jules G, Mowat, David, Plant, Gordon T, Robertson, Stephen P, Schorry, Elizabeth K, Scott, Richard H, Seaver, Laurie H, Sherr, Elliott, Splitt, Miranda, Stewart, Helen, Stumpel, Constance, Temel, Sehime G, Weaver, David D, Whiteford, Margo, Williams, Marc S, Tabor, Holly K, Smith, Joshua D, Shendure, Jay, Nickerson, Deborah A, Genomics, University of Washington Center for Mendelian, Bamshad, Michael J
المصدر: American Journal of Human Genetics. 94(5)
مصطلحات موضوعية: Rare Diseases, Human Genome, Genetics, Congenital Structural Anomalies, Pediatric, Dental/Oral and Craniofacial Disease, 2.1 Biological and endogenous factors, Aetiology, Congenital, Abnormalities, Multiple, Arachnodactyly, Arthrogryposis, Blepharophimosis, Child, Child, Preschool, Cleft Palate, Clubfoot, Connective Tissue Diseases, Contracture, Exome, Female, Hand Deformities, Congenital, Humans, Ion Channels, Male, Mutation, Ophthalmoplegia, Pedigree, Retinal Diseases, University of Washington Center for Mendelian Genomics, Biological Sciences, Medical and Health Sciences, Genetics & Heredity
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/2mm0j4f2
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6دورية أكاديمية
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7دورية أكاديمية
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8
المؤلفون: Ergoren, Mahmut C., Temel, Sehime G., Mocan, Gamze, Dundar, Munis
المصدر: Global Medical Genetics, Vol 08, Iss 02, Pp 069-071 (2021)
Global Medical Geneticsمصطلحات موضوعية: 0301 basic medicine, Thalassemia, media_common.quotation_subject, Immigration, malaria, QH426-470, genetic fitness, 03 medical and health sciences, Deportation, 0302 clinical medicine, ivs-ii-745, parasitic diseases, Genetics, medicine, Gene, Genotyping, RC254-282, media_common, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Grandparent, circassians, medicine.disease, 030104 developmental biology, Geography, β-thalassemia, Mutation (genetic algorithm), Original Article, cyprus, 030217 neurology & neurosurgery, Malaria, Demography
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::182367638636dec3da918220dad5f125
https://doi.org/10.1055/s-0041-1726336 -
9دورية أكاديمية
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10دورية أكاديمية
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تسجيل الدخول للوصول الكامل.