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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Disease and DFNB31[original query]
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. GWAS Catalog
Progress in neuro-psychopharmacology & biological psychiatry 2016 Feb 65 17-24.
Fabbri Chiara, Serretti Alessand
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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