Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: DFNB31[original query] |
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Sequence variants of the DFNB31 gene among Usher syndrome patients of diverse origin. Molecular vision 2010 16 495-500. Aller Elena, Jaijo Teresa, van Wijk Erwin, Ebermann Inga, Kersten Ferry, García-García Gema, Voesenek Krysta, Aparisi María José, Hoefsloot Lies, Cremers Cor, Díaz-Llopis Manuel, Pennings Ronald, Bolz Hanno J, Kremer Hannie, Millán José |
Nominal association between a polymorphism in DGKH and bipolar disorder detected in a meta-analysis of East Asian case-control samples. Psychiatry and clinical neurosciences 2011 Apr 65 (3): 280-5. Takata Atsushi, Kawasaki Hiroaki, Iwayama Yoshimi, Yamada Kazuo, Gotoh Leo, Mitsuyasu Hiroshi, Miura Tomofumi, Kato Tadafumi, Yoshikawa Takeo, Kanba Shigeno |
Novel chemosensitive single-nucleotide polymorphism markers to targeted regimens in metastatic colorectal cancer. Clinical cancer research : an official journal of the American Association for Cancer Research 2011 Mar 17 (5): 1200-9. Kim Jin C, Kim Seon Y, Cho Dong H, Ha Ye J, Choi Eun Y, Kim Chan W, Roh Seon A, Kim Tae W, Ju Hyoungseok, Kim Yong |
Targeted next generation sequencing for molecular diagnosis of Usher syndrome. Orphanet journal of rare diseases 2014 9 168. Aparisi María J, Aller Elena, Fuster-García Carla, García-García Gema, Rodrigo Regina, Vázquez-Manrique Rafael P, Blanco-Kelly Fiona, Ayuso Carmen, Roux Anne-Françoise, Jaijo Teresa, Millán José |
Comprehensive molecular diagnosis of 67 Chinese Usher syndrome probands: high rate of ethnicity specific mutations in Chinese USH patients. Orphanet journal of rare diseases 2015 10 (1): 110. Jiang Lichun, Liang Xiaofang, Li Yumei, Wang Jing, Zaneveld Jacques Eric, Wang Hui, Xu Shan, Wang Keqing, Wang Binbin, Chen Rui, Sui Ruifa |
Genetics of long-term treatment outcome in bipolar disorder.
Progress in neuro-psychopharmacology & biological psychiatry 2016 Feb 65 17-24. Fabbri Chiara, Serretti Alessand |
Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss. PloS one 2015 10 (11): e0142154. Atik Tahir, Onay Huseyin, Aykut Ayca, Bademci Guney, Kirazli Tayfun, Tekin Mustafa, Ozkinay Fer |
Association of established hypothyroidism-associated genetic variants with Hashimoto's thyroiditis. Journal of endocrinological investigation 2017 Apr . Bari? A, Br?i? L, Gra?an S, Torlak Lovri? V, Gunja?a I, Šimunac M, Brekalo M, Boban M, Polašek O, Barbali? M, Zemunik T, Punda A, Boraska Perica |
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