Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Syndrome and AOS[original query] |
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SMAD3 is associated with the total burden of radiographic osteoarthritis: the Chingford study. PloS one 2014 9 (5): e97786. Aref-Eshghi Erfan, Zhang Yuhua, Hart Deborah, Valdes Ana M, Furey Andrew, Martin Glynn, Sun Guang, Rahman Proton, Arden Nigel, Spector Tim D, Zhai Guang |
Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams-Oliver Syndrome With Variable Cardiac Anomalies. Circulation. Cardiovascular genetics 2015 Aug 8 (4): 572-81. Southgate Laura, Sukalo Maja, Karountzos Anastasios S V, Taylor Edward J, Collinson Claire S, Ruddy Deborah, Snape Katie M, Dallapiccola Bruno, Tolmie John L, Joss Shelagh, Brancati Francesco, Digilio Maria Cristina, Graul-Neumann Luitgard M, Salviati Leonardo, Coerdt Wiltrud, Jacquemin Emmanuel, Wuyts Wim, Zenker Martin, Machado Rajiv D, Trembath Richard |
Prognostic significance of histomolecular subgroups of adult anaplastic (WHO Grade III) gliomas: applying the 'integrated' diagnosis approach. Journal of clinical pathology 2016 Jan . Rajmohan K S, Sugur Harsha S, Shwetha S D, Ramesh Arvind, Thennarasu Kandavel, Pandey Paritosh, Arivazhagan Arimappamagan, Santosh Va |
Elucidating the genetic architecture of Adams-Oliver syndrome in a large European cohort. Human mutation 2018 Jun . Meester Josephina A N, Sukalo Maja, Schröder Kim C, Schanze Denny, Baynam Gareth, Borck Guntram, Bramswig Nuria C, Duman Duygu, Gilbert-Dussardier Brigitte, Holder-Espinasse Muriel, Itin Peter, Johnson Diana S, Joss Shelagh, Koillinen Hannele, McKenzie Fiona, Morton Jenny, Nelle Heike, Reardon Willie, Roll Claudia, Salih Mustafa A, Savarirayan Ravi, Scurr Ingrid, Splitt Miranda, Thompson Elizabeth, Titheradge Hannah, Travers Colm P, Van Maldergem Lionel, Whiteford Margo, Wieczorek Dagmar, Vandeweyer Geert, Trembath Richard, Van Laer Lut, Loeys Bart L, Zenker Martin, Southgate Laura, Wuyts W |
Epileptic Encephalopathy in Adams-Oliver Syndrome Associated to a New DOCK6 Mutation: A Peculiar Behavioral Phenotype. Neuropediatrics 2018 4 49 (3): 217-221. Pisciotta Livia, Capra Valeria, Accogli Andrea, Giacomini Thea, Prato Giulia, Tavares Purificação, Pinto-Basto Jorge, Morana Giovanni, Mancardi Maria Margheri |
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- Page last updated:May 06, 2024
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