Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: RAP1GDS1[original query] |
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Genome-wide association study of biochemical traits in Korcula Island, Croatia.
Croatian medical journal 2009 Feb 50 (1): 23-33. Zemunik Tatijana, Boban Mladen, Lauc Gordan, Jankovi? Stipan, Rotim Kresimir, Vatavuk Zoran, Benci? Goran, Dogas Zoran, Boraska Vesna, Torlak Vesela, Susac Jelena, Zobi? Ivana, Rudan Diana, Pulani? Drazen, Modun Darko, Mudni? Ivana, Gunjaca Grgo, Budimir Danijela, Hayward Caroline, Vitart Veronique, Wright Alan F, Campbell Harry, Rudan Ig |
Mutations in RABL3 alter KRAS prenylation and are associated with hereditary pancreatic cancer. Nature genetics 2019 8 51 (9): 1308-1314. Nissim Sahar, Leshchiner Ignaty, Mancias Joseph D, Greenblatt Matthew B, Maertens Ophélia, Cassa Christopher A, Rosenfeld Jill A, Cox Andrew G, Hedgepeth John, Wucherpfennig Julia I, Kim Andrew J, Henderson Jake E, Gonyo Patrick, Brandt Anthony, Lorimer Ellen, Unger Bethany, Prokop Jeremy W, Heidel Jerry R, Wang Xiao-Xu, Ukaegbu Chinedu I, Jennings Benjamin C, Paulo Joao A, Gableske Sebastian, Fierke Carol A, Getz Gad, Sunyaev Shamil R, Wade Harper J, Cichowski Karen, Kimmelman Alec C, Houvras Yariv, Syngal Sapna, Williams Carol, Goessling Wolfr |
Mutated RAP1GDS1 causes a new syndrome of dysmorphic feature, intellectual disability & speech delay. Annals of clinical and translational neurology 2020 5 7 (6): 956-964. Asiri Abdulaziz, Aloyouni Essra, Umair Muhammad, Alyafee Yusra, Al Tuwaijri Abeer, Alhamoudi Kheloud M, Almuzzaini Bader, Al Baz Abeer, Alwadaani Deemah, Nashabat Marwan, Alfadhel Maj |
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