Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: HOXB1[original query] |
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Candidate gene study of HOXB1 in autism spectrum disorder. Molecular autism 2010 1 (1): 9. Muscarella Lucia A, Guarnieri Vito, Sacco Roberto, Curatolo Paolo, Manzi Barbara, Alessandrelli Riccardo, Giana Grazia, Militerni Roberto, Bravaccio Carmela, Lenti Carlo, Saccani Monica, Schneider Cindy, Melmed Raun, D'Agruma Leonardo, Persico Antonio |
An integrated meta-analysis of two variants in HOXA1/HOXB1 and their effect on the risk of autism spectrum disorders. PloS one 2011 6 (9): e25603. Song Ran-Ran, Zou Li, Zhong Rong, Zheng Xia-Wen, Zhu Bei-Bei, Chen Wei, Liu Li, Miao Xiao-Pi |
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations. American journal of human genetics 2017 Nov 101 (5): 789-802. Sanna-Cherchi Simone, Khan Kamal, Westland Rik, Krithivasan Priya, Fievet Lorraine, Rasouly Hila Milo, Ionita-Laza Iuliana, Capone Valentina P, Fasel David A, Kiryluk Krzysztof, Kamalakaran Sitharthan, Bodria Monica, Otto Edgar A, Sampson Matthew G, Gillies Christopher E, Vega-Warner Virginia, Vukojevic Katarina, Pediaditakis Igor, Makar Gabriel S, Mitrotti Adele, Verbitsky Miguel, Martino Jeremiah, Liu Qingxue, Na Young-Ji, Goj Vinicio, Ardissino Gianluigi, Gigante Maddalena, Gesualdo Loreto, Janezcko Magdalena, Zaniew Marcin, Mendelsohn Cathy Lee, Shril Shirlee, Hildebrandt Friedhelm, van Wijk Joanna A E, Arapovic Adela, Saraga Marijan, Allegri Landino, Izzi Claudia, Scolari Francesco, Tasic Velibor, Ghiggeri Gian Marco, Latos-Bielenska Anna, Materna-Kiryluk Anna, Mane Shrikant, Goldstein David B, Lifton Richard P, Katsanis Nicholas, Davis Erica E, Gharavi Ali |
Analysis of HOXB1 gene in a cohort of patients with sporadic ventricular septal defect. Molecular biology reports 2018 Jun . Pinard Amélie, Eudes Nathalie, Mitchell Julia, Bajolle Fanny, Grelet Maude, Okoronkwo Joséphine, Bonnet Damien, Collod-Béroud Gwenaelle, Zaffran Stépha |
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