Derti A, Roth FP, Church GM, Wu CT (October 2006). "Mammalian ultraconserved elements are strongly depleted among segmental duplications and copy number variants". Nature Genetics. 38 (10): 1216–1220. doi:10.1038/ng1888. PMID16998490. S2CID10671674.
Fodde R, van der Luijt R, Wijnen J, Tops C, van der Klift H, van Leeuwen-Cornelisse I, et al. (August 1992). "Eight novel inactivating germ line mutations at the APC gene identified by denaturing gradient gel electrophoresis". Genomics. 13 (4): 1162–1168. doi:10.1016/0888-7543(92)90032-n. PMID1324223.
Grauers A, Wang J, Einarsdottir E, Simony A, Danielsson A, Åkesson K, et al. (October 2015). "Candidate gene analysis and exome sequencing confirm LBX1 as a susceptibility gene for idiopathic scoliosis". The Spine Journal. 15 (10): 2239–2246. doi:10.1016/j.spinee.2015.05.013. hdl:10616/44765. PMID25987191.
Londono D, Kou I, Johnson TA, Sharma S, Ogura Y, Tsunoda T, et al. (June 2014). "A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups". Journal of Medical Genetics. 51 (6): 401–406. doi:10.1136/jmedgenet-2013-102067. PMID24721834. S2CID23646905.
Jiang Y, Ben Q, Shen H, Lu W, Zhang Y, Zhu J (November 2011). "Diabetes mellitus and incidence and mortality of colorectal cancer: a systematic review and meta-analysis of cohort studies". European Journal of Epidemiology. 26 (11): 863–876. doi:10.1007/s10654-011-9617-y. PMID21938478. S2CID99605.
Takahashi Y, Kou I, Takahashi A, Johnson TA, Kono K, Kawakami N, et al. (October 2011). "A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis". Nature Genetics. 43 (12): 1237–1240. doi:10.1038/ng.974. PMID22019779. S2CID7533298.
Gorman MP, Golomb MR, Walsh LE, Hobson GM, Garbern JY, Kinkel RP, et al. (April 2007). "Steroid-responsive neurologic relapses in a child with a proteolipid protein-1 mutation". Neurology. 68 (16): 1305–1307. doi:10.1212/01.wnl.0000259522.49388.53. PMID17438221. S2CID45639125.
Saugier-Veber P, Munnich A, Bonneau D, Rozet JM, Le Merrer M, Gil R, Boespflug-Tanguy O (March 1994). "X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus". Nature Genetics. 6 (3): 257–262. doi:10.1038/ng0394-257. PMID8012387. S2CID13607673.
Knoblauch H, Geier C, Adams S, Budde B, Rudolph A, Zacharias U, et al. (January 2010). "Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation". Annals of Neurology. 67 (1): 136–140. doi:10.1002/ana.21839. PMID20186852. S2CID30441775.
Schoser B, Goebel HH, Janisch I, Quasthoff S, Rother J, Bergmann M, et al. (August 2009). "Consequences of mutations within the C terminus of the FHL1 gene". Neurology. 73 (7): 543–551. doi:10.1212/WNL.0b013e3181b2a4b3. PMID19687455. S2CID13107330.
Grauers A, Wang J, Einarsdottir E, Simony A, Danielsson A, Åkesson K, et al. (October 2015). "Candidate gene analysis and exome sequencing confirm LBX1 as a susceptibility gene for idiopathic scoliosis". The Spine Journal. 15 (10): 2239–2246. doi:10.1016/j.spinee.2015.05.013. hdl:10616/44765. PMID25987191.
Derti A, Roth FP, Church GM, Wu CT (October 2006). "Mammalian ultraconserved elements are strongly depleted among segmental duplications and copy number variants". Nature Genetics. 38 (10): 1216–1220. doi:10.1038/ng1888. PMID16998490. S2CID10671674.
Fodde R, van der Luijt R, Wijnen J, Tops C, van der Klift H, van Leeuwen-Cornelisse I, et al. (August 1992). "Eight novel inactivating germ line mutations at the APC gene identified by denaturing gradient gel electrophoresis". Genomics. 13 (4): 1162–1168. doi:10.1016/0888-7543(92)90032-n. PMID1324223.
Grauers A, Wang J, Einarsdottir E, Simony A, Danielsson A, Åkesson K, et al. (October 2015). "Candidate gene analysis and exome sequencing confirm LBX1 as a susceptibility gene for idiopathic scoliosis". The Spine Journal. 15 (10): 2239–2246. doi:10.1016/j.spinee.2015.05.013. hdl:10616/44765. PMID25987191.
Londono D, Kou I, Johnson TA, Sharma S, Ogura Y, Tsunoda T, et al. (June 2014). "A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups". Journal of Medical Genetics. 51 (6): 401–406. doi:10.1136/jmedgenet-2013-102067. PMID24721834. S2CID23646905.
Jiang Y, Ben Q, Shen H, Lu W, Zhang Y, Zhu J (November 2011). "Diabetes mellitus and incidence and mortality of colorectal cancer: a systematic review and meta-analysis of cohort studies". European Journal of Epidemiology. 26 (11): 863–876. doi:10.1007/s10654-011-9617-y. PMID21938478. S2CID99605.
Takahashi Y, Kou I, Takahashi A, Johnson TA, Kono K, Kawakami N, et al. (October 2011). "A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis". Nature Genetics. 43 (12): 1237–1240. doi:10.1038/ng.974. PMID22019779. S2CID7533298.
Gorman MP, Golomb MR, Walsh LE, Hobson GM, Garbern JY, Kinkel RP, et al. (April 2007). "Steroid-responsive neurologic relapses in a child with a proteolipid protein-1 mutation". Neurology. 68 (16): 1305–1307. doi:10.1212/01.wnl.0000259522.49388.53. PMID17438221. S2CID45639125.
Saugier-Veber P, Munnich A, Bonneau D, Rozet JM, Le Merrer M, Gil R, Boespflug-Tanguy O (March 1994). "X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus". Nature Genetics. 6 (3): 257–262. doi:10.1038/ng0394-257. PMID8012387. S2CID13607673.
Knoblauch H, Geier C, Adams S, Budde B, Rudolph A, Zacharias U, et al. (January 2010). "Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation". Annals of Neurology. 67 (1): 136–140. doi:10.1002/ana.21839. PMID20186852. S2CID30441775.
Schoser B, Goebel HH, Janisch I, Quasthoff S, Rother J, Bergmann M, et al. (August 2009). "Consequences of mutations within the C terminus of the FHL1 gene". Neurology. 73 (7): 543–551. doi:10.1212/WNL.0b013e3181b2a4b3. PMID19687455. S2CID13107330.
Derti A, Roth FP, Church GM, Wu CT (October 2006). "Mammalian ultraconserved elements are strongly depleted among segmental duplications and copy number variants". Nature Genetics. 38 (10): 1216–1220. doi:10.1038/ng1888. PMID16998490. S2CID10671674.
Londono D, Kou I, Johnson TA, Sharma S, Ogura Y, Tsunoda T, et al. (June 2014). "A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups". Journal of Medical Genetics. 51 (6): 401–406. doi:10.1136/jmedgenet-2013-102067. PMID24721834. S2CID23646905.
Jiang Y, Ben Q, Shen H, Lu W, Zhang Y, Zhu J (November 2011). "Diabetes mellitus and incidence and mortality of colorectal cancer: a systematic review and meta-analysis of cohort studies". European Journal of Epidemiology. 26 (11): 863–876. doi:10.1007/s10654-011-9617-y. PMID21938478. S2CID99605.
Takahashi Y, Kou I, Takahashi A, Johnson TA, Kono K, Kawakami N, et al. (October 2011). "A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis". Nature Genetics. 43 (12): 1237–1240. doi:10.1038/ng.974. PMID22019779. S2CID7533298.
Gorman MP, Golomb MR, Walsh LE, Hobson GM, Garbern JY, Kinkel RP, et al. (April 2007). "Steroid-responsive neurologic relapses in a child with a proteolipid protein-1 mutation". Neurology. 68 (16): 1305–1307. doi:10.1212/01.wnl.0000259522.49388.53. PMID17438221. S2CID45639125.
Saugier-Veber P, Munnich A, Bonneau D, Rozet JM, Le Merrer M, Gil R, Boespflug-Tanguy O (March 1994). "X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus". Nature Genetics. 6 (3): 257–262. doi:10.1038/ng0394-257. PMID8012387. S2CID13607673.
Knoblauch H, Geier C, Adams S, Budde B, Rudolph A, Zacharias U, et al. (January 2010). "Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation". Annals of Neurology. 67 (1): 136–140. doi:10.1002/ana.21839. PMID20186852. S2CID30441775.
Schoser B, Goebel HH, Janisch I, Quasthoff S, Rother J, Bergmann M, et al. (August 2009). "Consequences of mutations within the C terminus of the FHL1 gene". Neurology. 73 (7): 543–551. doi:10.1212/WNL.0b013e3181b2a4b3. PMID19687455. S2CID13107330.