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1دورية أكاديمية
المؤلفون: Ryan, Charles W.Aff1, Aff2, Peirent, Emily R., Regan, Samantha L., Guxholli, AlbaAff4, Aff5, Bielas, Stephanie L.Aff1, Aff3, Aff4, Aff5, IDs0043902302557x_cor5
المصدر: Human Genetics. 143(4):511-527
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2دورية أكاديمية
المؤلفون: Werren, Elizabeth A.Aff1, Aff2, Peirent, Emily R., Jantti, Henna, Guxholli, AlbaAff1, Aff5, Srivastava, Kinshuk Raj, Orenstein, Naama, Narayanan, Vinodh, Wiszniewski, Wojciech, Dawidziuk, Mateusz, Gawlinski, Pawel, Umair, MuhammadAff11, Aff12, Khan, AmjadAff9, Aff13, Khan, Shahid Niaz, Geneviève, David, Lehalle, Daphné, van Gassen, K. L. I., Giltay, Jacques C., Oegema, Renske, van Jaarsveld, Richard H., Rafiullah, Rafiullah, Rappold, Gudrun A., Rabin, Rachel, Pappas, John G., Wheeler, Marsha M., Bamshad, Michael J.Aff22, Aff23, Tsan, Yao-Chang, Johnson, Matthew B., Keegan, Catherine E.Aff1, Aff5, Srivastava, AnshikaAff25, IDs41419024067686_cor29, Bielas, Stephanie L.Aff1, Aff5, IDs41419024067686_cor30
المصدر: Cell Death & Disease. 15(5)
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3دورية أكاديمية
المؤلفون: Khoa, Le Tran PhucAff1, Aff7, Yang, Wentao, Shan, Mengrou, Zhang, Li, Mao, Fengbiao, Zhou, Bo, Li, Qiang, Malcore, Rebecca, Harris, Clair, Zhao, Lili, Rao, Rajesh C., Iwase, Shigeki, Kalantry, Sundeep, Bielas, Stephanie L., Lyssiotis, Costas A., Dou, YaliAff1, IDs41467024465664_cor16
المصدر: Nature Communications. 15(1)
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4دورية أكاديمية
المؤلفون: Khoa, Le Tran PhucAff1, Aff7, Yang, Wentao, Shan, Mengrou, Zhang, Li, Mao, Fengbiao, Zhou, Bo, Li, Qiang, Malcore, Rebecca, Harris, Clair, Zhao, Lili, Rao, Rajesh C., Iwase, Shigeki, Kalantry, Sundeep, Bielas, Stephanie L., Lyssiotis, Costas A., Dou, YaliAff1, IDs41467024461211_cor16
المصدر: Nature Communications. 15(1)
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5دورية أكاديمية
المؤلفون: Werren, Elizabeth A.Aff1, Aff2, LaForce, Geneva R., Srivastava, AnshikaAff1, Aff4, Perillo, Delia R., Li, Shaokun, Johnson, Katherine, Baris, Safa, Berger, Brandon, Regan, Samantha L., Pfennig, Christian D., de Munnik, Sonja, Pfundt, Rolph, Hebbar, Malavika, Jimenez-Heredia, Raúl, Karakoc-Aydiner, Elif, Ozen, Ahmet, Dmytrus, Jasmin, Krolo, Ana, Corning, Ken, Prijoles, E. J., Louie, Raymond J., Lebel, Robert Roger, Le, Thuy-Linh, Amiel, JeanneAff12, Aff13, Gordon, Christopher T., Boztug, KaanAff8, Aff9, Aff14, Aff15, Girisha, Katta M., Shukla, Anju, Bielas, Stephanie L.Aff1, Aff17, IDs4146702445948y_cor29, Schaffer, Ashleigh E.Aff3, IDs4146702445948y_cor30
المصدر: Nature Communications. 15(1)
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6دورية أكاديمية
المؤلفون: Werren, Elizabeth A., Guxholli, Alba, Jones, Natasha, Wagner, Matias, Hannibal, Iris, Granadillo, Jorge L., Tyndall, Amanda V., Moccia, Amanda, Kuehl, Ryan, Levandoski, Kristin M., Day-Salvatore, Debra L., Wheeler, Marsha, Chong, Jessica X., Bamshad, Michael J., Innes, A. Micheil, Pierson, Tyler Mark, Mackay, Joel P., Bielas, Stephanie L., Martin, Donna M.
المصدر: In Human Genetics and Genomics Advances 13 July 2023 4(3)
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7دورية أكاديمية
المؤلفون: Boda, EnricaAff1, Aff2, IDs41467022300106_cor1, Lorenzati, MartinaAff1, Aff2, Parolisi, RobertaAff1, Aff2, Harding, Brian, Pallavicini, GianmarcoAff1, Aff2, Bonfanti, LucaAff2, Aff4, Moccia, Amanda, Bielas, Stephanie, Di Cunto, FerdinandoAff1, Aff2, Buffo, AnnalisaAff1, Aff2
المصدر: Nature Communications. 13(1)
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8دورية أكاديمية
المؤلفون: Narayanan, Dhanya Lakshmi, Udyawar, Divya, Kaur, Parneet, Sharma, Suvasini, Suresh, Narayanaswamy, Nampoothiri, Sheela, do Rosario, Michelle C., Somashekar, Puneeth H., Rao, Lakshmi Priya, Kausthubham, Neethukrishna, Majethia, Purvi, Pande, Shruti, Ramesh Bhat, Y., Shrikiran, Aroor, Bielas, Stephanie, Girisha, Katta Mohan, Shukla, AnjuAff1
المصدر: European Journal of Human Genetics. 29(12):1774-1780
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9دورية أكاديمية
المؤلفون: Jordan, Valerie K, Fregeau, Brieana, Ge, Xiaoyan, Giordano, Jessica, Wapner, Ronald J, Balci, Tugce B, Carter, Melissa T, Bernat, John A, Moccia, Amanda N, Srivastava, Anshika, Martin, Donna M, Bielas, Stephanie L, Pappas, John, Svoboda, Melissa D, Rio, Marlène, Boddaert, Nathalie, Cantagrel, Vincent, Lewis, Andrea M, Scaglia, Fernando, Network, Undiagnosed Diseases, Kohler, Jennefer N, Bernstein, Jonathan A, Dries, Annika M, Rosenfeld, Jill A, DeFilippo, Colette, Thorson, Willa, Yang, Yaping, Sherr, Elliott H, Bi, Weimin, Scott, Daryl A
المصدر: Human Mutation. 39(5)
مصطلحات موضوعية: Congenital Structural Anomalies, Genetics, Genetic Testing, Rare Diseases, Pediatric, Aetiology, 2.1 Biological and endogenous factors, Adolescent, Carrier Proteins, Child, Preschool, Fatal Outcome, Female, Genetic Association Studies, Humans, Infant, Male, Mutation, Young Adult, 1p36 deletion syndrome, CHARGE syndrome, CHD7, genotype-phenotype correlations, NEDBEH, RERE, Undiagnosed Diseases Network, Clinical Sciences, Genetics & Heredity
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/57z6f57h
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10دورية أكاديمية
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