Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: HOXA2[original query] |
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HOXA2 haploinsufficiency in dominant bilateral microtia and hearing loss. Human mutation 2013 Oct 34 (10): 1347-51. Brown Kerry K, Viana Lucas M, Helwig Cecilia C, Artunduaga Maria A, Quintanilla-Dieck Lourdes, Jarrin Patricia, Osorno Gabriel, McDonough Barbara, DePalma Steven R, Eavey Roland D, Seidman Jonathan G, Seidman Christine |
Genetic association of ARHGAP21 gene variant with mandibular prognathism. Journal of dental research 2015 Apr 94 (4): 569-76. Perillo L, Monsurrò A, Bonci E, Torella A, Mutarelli M, Nigro |
Mutational analysis of GSC, HOXA2 and PRKRA in 106 Chinese patients with microtia. International journal of pediatric otorhinolaryngology 2017 1 93 78-82. Hao Shaojuan, Jin Lei, Li Chenlong, Wang Huijun, Zheng Fengyun, Ma Duan, Zhang Tian |
Biology and Clinical Implications of the 19q13 Aggressive Prostate Cancer Susceptibility Locus. Cell 2018 7 174 (3): 576-589.e18. Gao Ping, Xia Ji-Han, Sipeky Csilla, Dong Xiao-Ming, Zhang Qin, Yang Yuehong, Zhang Peng, Cruz Sara Pereira, Zhang Kai, Zhu Jing, Lee Hang-Mao, Suleman Sufyan, Giannareas Nikolaos, Liu Song, , Tammela Teuvo L J, Auvinen Anssi, Wang Xiaoyue, Huang Qilai, Wang Liguo, Manninen Aki, Vaarala Markku H, Wang Liang, Schleutker Johanna, Wei Gong-Ho |
The Enigmatic Etiology of Oculo-Auriculo-Vertebral Spectrum (OAVS): An Exploratory Gene Variant Interaction Approach in Candidate Genes. Life (Basel, Switzerland) 2022 11 12 (11): . Estandia-Ortega Bernardette, Reyna-Fabián Miriam Erandi, Velázquez-Aragón José Antonio, González-Del Angel Ariadna, Fernández-Hernández Liliana, Alcántara-Ortigoza Miguel Ang |
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