Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: PNPLA4[original query] |
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Genetic variance in the adiponutrin gene family and childhood obesity. PloS one 2009 4 (4): e5327. Johansson Lovisa E, Johansson Lina M, Danielsson Pernilla, Norgren Svante, Johansson Stina, Marcus Claude, Ridderstråle Mart |
Exome sequencing identified a de novo mutation of PURA gene in a patient with familial Xp22.31 microduplication. European journal of medical genetics 2018 6 62 (2): 103-108. Qiao Ying, Bagheri Hani, Tang Flamingo, Badduke Chansonette, Martell Sally, Lewis Suzanne M E, Robinson Wendy, Connolly Mary B, Arbour Laura, Rajcan-Separovic Evi |
Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysis. BMC medical genetics 2018 3 19 (1): 46. Prasad Aparna, Sdano Matthew A, Vanzo Rena J, Mowery-Rushton Patricia A, Serrano Moises A, Hensel Charles H, Wassman E Robe |
A prenatal diagnosis and genetics study of five pedigrees in the Chinese population with Xp22.31 microduplication. Molecular cytogenetics 2019 12 12 50. Zhuang Jianlong, Wang Yuanbai, Zeng Shuhong, Lv Chunling, Lin Yiming, Jiang Yuyi |
Characterising heart rhythm abnormalities associated with Xp22.31 deletion. Journal of medical genetics 2022 11 . Wren Georgina, Baker Emily, Underwood Jack, Humby Trevor, Thompson Andrew, Kirov George, Escott-Price Valentina, Davies Willi |
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