Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: IMPG1[original query] |
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Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan.
PloS one 2009 4 (5): e5459. Yang Hsin-Chou, Liang Yu-Jen, Wu Yi-Lin, Chung Chia-Min, Chiang Kuang-Mao, Ho Hung-Yun, Ting Chih-Tai, Lin Tsung-Hsien, Sheu Sheng-Hsiung, Tsai Wei-Chuan, Chen Jyh-Hong, Leu Hsin-Bang, Yin Wei-Hsian, Chiu Ting-Yu, Chen Chin-Iuan, Fann Cathy S J, Wu Jer-Yuarn, Lin Teng-Nan, Lin Shing-Jong, Chen Yuan-Tsong, Chen Jaw-Wen, Pan Wen-Ha |
Evaluation of the association of single nucleotide polymorphisms in the PRPH2 gene with adult-onset foveomacular vitelliform dystrophy. Ophthalmic genetics 2016 Feb 1-5. Grunin Michelle, Tiosano Liran, Jaouni Tareq, Averbukh Edward, Sharon Dror, Chowers It |
ADULT-ONSET VITELLIFORM MACULAR DYSTROPHY SECONDARY TO A NOVEL IMPG2 GENE VARIANT. Retinal cases & brief reports 2018 10 15 (4): 356-358. Shah Saumya M, Schimmenti Lisa A, Marmorstein Alan D, Bakri Sophie |
Identification of MYO6 copy number variation associated with cochlear aplasia by targeted sequencing. International journal of pediatric otorhinolaryngology 2019 12 128 109689. Sun Lianhua, Wang Xiaowen, Hou Shule, Liang Min, Yang J |
Novel IMPG2 variant causing adult macular vitelliform dystrophy: A case report. European journal of ophthalmology 2023 9 11206721231199850. Nicolò Ribarich, Maria Chiara Rivolta, Riccardo Sacconi, Giuseppe Querqu |
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