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Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...Nature medicine, 2019-06, Vol.25 (6), p.911-919
- Frésard, Laure
- Smail, Craig
- Ferraro, Nicole M.
- Teran, Nicole A.
- Li, Xin
- Smith, Kevin S.
- Bonner, Devon
- Kernohan, Kristin D.
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- Balliu, Brunilda
- Davis, Joe R.
- Liu, Boxiang
- Prybol, Cameron J.
- Kohler, Jennefer N.
- Zastrow, Diane B.
- Reuter, Chloe M.
- Fisk, Dianna G.
- Grove, Megan E.
- Davidson, Jean M.
- Hartley, Taila
- Joshi, Ruchi
- Strober, Benjamin J.
- Utiramerur, Sowmithri
- Lind, Lars
- Ingelsson, Erik
- Battle, Alexis
- Bejerano, Gill
- Bernstein, Jonathan A.
- Ashley, Euan A.
- Boycott, Kym M.
- Merker, Jason D.
- Wheeler, Matthew T.
- Montgomery, Stephen B.
2019
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The New England journal of medicine, 2018-11, Vol.379 (22), p.2131-2139
- Splinter, Kimberly
- Adams, David R
- Bacino, Carlos A
- Bellen, Hugo J
- Bernstein, Jonathan A
- Cheatle-Jarvela, Alys M
- Eng, Christine M
- Esteves, Cecilia
- Gahl, William A
- Hamid, Rizwan
- Jacob, Howard J
- Kikani, Bijal
- Koeller, David M
- Kohane, Isaac S
- Lee, Brendan H
- Loscalzo, Joseph
- Luo, Xi
- McCray, Alexa T
- Metz, Thomas O
- Mulvihill, John J
- Nelson, Stanley F
- Palmer, Christina G.S
- Phillips, John A
- Pick, Leslie
- Postlethwait, John H
- Reuter, Chloe
- Shashi, Vandana
- Sweetser, David A
- Tifft, Cynthia J
- Walley, Nicole M
- Wangler, Michael F
- Westerfield, Monte
- Wheeler, Matthew T
- Wise, Anastasia L
- Worthey, Elizabeth A
- Yamamoto, Shinya
- Ashley, Euan A
2018
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Journal of acquired immune deficiency syndromes (1999), 2021-08, Vol.87 (Suppl 1), p.S6-S16
- Sachathep, Karampreet
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American journal of human genetics, 2020-04, Vol.106 (4), p.570-583
- Mao, Dongxue
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- Rosenfeld, Jill A.
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2020
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American journal of human genetics, 2017-01, Vol.100 (1), p.128-137
- Davids, Mariska
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- Pena, Loren D.M.
- Phillips, John A.
- Posey, Jennifer E.
- Potocki, Lorraine
- Pusey, Barbara N.
- Schoch, Kelly
- Scott, Daryl A.
- Sharma, Prashant
- Soldatos, Ariane G.
- Splinter, Kimberly
- Strong, Kimberly A.
- Sullivan, Jennifer A.
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- Thomas, Sara P.
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- Tolman, Nathanial J.
- Toro, Camilo
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- Webb-Robertson, Bobbie-Jo M.
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- Westerfield, Monte
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2017
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American journal of human genetics, 2018-03, Vol.102 (3), p.494-504
- Yoon, Wan Hee
- Jangam, Sharayu
- Davidson, Jean M.
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- Zhao, Chunli
- Contrepois, Kévin
- Heyman, Heino M.
- Webb-Robertson, Bobbie-Jo M.
- Alejandro, Mercedes E.
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- Balasubramanyam, Ashok
- Barseghyan, Hayk
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- Brush, Matthew
- Burke, Elizabeth A.
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- Cooper, Cynthia M.
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- Craigen, William J.
- D’Souza, Precilla
- Dayal, Jyoti G.
- Dell’Angelica, Esteban C.
- Dorset, Daniel C.
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- Eckstein, David J.
- Emrick, Lisa T.
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- Ferreira, Carlos
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- Gould, Sarah E.
- Gourdine, Jean-Philippe F.
- Hanchard, Neil A.
- Herzog, Matthew R.
- Hom, Jason
- Howerton, Ellen M.
- Huang, Yong
- Jacob, Howard J.
- Jiang, Yong-hui
- Johnston, Jean M.
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- Kohane, Isaac S.
- Krier, Joel B.
- Lazar, Jozef
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- MacRae, Calum A.
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2018
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American journal of human genetics, 2019-01, Vol.104 (1), p.164-178
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2019
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American journal of human genetics, 2019-08, Vol.105 (2), p.413-424
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2019
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Epilepsia (Copenhagen), 2019-03, Vol.60 (3), p.406-418
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2019
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AIDS (London), 2021-03, Vol.35 (4), p.585-594
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Orphanet journal of rare diseases, 2023-04, Vol.18 (1), p.73-10, Article 73
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2023
Volltextzugriff (PDF)
American journal of medical genetics. Part A, 2024-06, Vol.194 (6), p.e63556-n/a
- Forghani, Irman
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- Cogan, Joy D.
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- D'Souza, Precilla
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- Dell'Angelica, Esteban C.
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- Jamal, Fariha
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Orphanet journal of rare diseases, 2023-01, Vol.18 (1), p.6-8, Article 6
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