Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: PRTG[original query] |
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Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region. Genes, brain, and behavior 2008 Nov 7 (8): 877-86. Wigg K G, Feng Y, Crosbie J, Tannock R, Kennedy J L, Ickowicz A, Malone M, Schachar R, Barr C |
Association studies of low-frequency coding variants in nonsyndromic cleft lip with or without cleft palate. American journal of medical genetics. Part A 2017 Apr . Leslie Elizabeth J, Carlson Jenna C, Shaffer John R, Buxó Carmen J, Castilla Eduardo E, Christensen Kaare, Deleyiannis Frederic W B, Field Leigh L, Hecht Jacqueline T, Moreno Lina, Orioli Ieda M, Padilla Carmencita, Vieira Alexandre R, Wehby George L, Feingold Eleanor, Weinberg Seth M, Murray Jeffrey C, Marazita Mary |
Validation of loci at 2q14.2 and 15q21.3 as risk factors for testicular cancer. Oncotarget 2018 Feb 9 (16): 12630-12638. Loveday Chey, Litchfield Kevin, Levy Max, Holroyd Amy, Broderick Peter, Kote-Jarai Zsofia, Dunning Alison M, Muir Kenneth, Peto Julian, Eeles Rosalind, Easton Douglas F, Dudakia Darshna, Orr Nick, Pashayan Nora, Reid Alison, Huddart Robert A, Houlston Richard S, Turnbull Cla |
In trans variant calling reveals enrichment for compound heterozygous variants in genes involved in neuronal development and growth. Genetics research 2019 6 101 e8. Cox Allison J, Grady Fillan, Velez Gabriel, Mahajan Vinit B, Ferguson Polly J, Kitchen Andrew, Darbro Benjamin W, Bassuk Alexander |
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- Page last updated:Apr 16, 2024
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