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IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome.
Tyson J, Tranebjaerg L, Bellman S, Wren C, Taylor JF, Bathen J, Aslaksen B, Sørland SJ, Lund O, Malcolm S, Pembrey M, Bhattacharya S, Bitner-Glindzicz M. Tyson J, et al. Among authors: taylor jf. Hum Mol Genet. 1997 Nov;6(12):2179-85. doi: 10.1093/hmg/6.12.2179. Hum Mol Genet. 1997. PMID: 9328483
A prospective cytogenetic study of 36 cases of DiGeorge syndrome.
Wilson DI, Cross IE, Goodship JA, Brown J, Scambler PJ, Bain HH, Taylor JF, Walsh K, Bankier A, Burn J, et al. Wilson DI, et al. Among authors: taylor jf. Am J Hum Genet. 1992 Nov;51(5):957-63. Am J Hum Genet. 1992. PMID: 1415264 Free PMC article.
Alström syndrome. Report of 22 cases and literature review.
Russell-Eggitt IM, Clayton PT, Coffey R, Kriss A, Taylor DS, Taylor JF. Russell-Eggitt IM, et al. Among authors: taylor jf, taylor ds. Ophthalmology. 1998 Jul;105(7):1274-80. doi: 10.1016/S0161-6420(98)97033-6. Ophthalmology. 1998. PMID: 9663233 Review.
Leber's congenital amaurosis--a new syndrome with a cardiomyopathy.
Russell-Eggitt IM, Taylor DS, Clayton PT, Garner A, Kriss A, Taylor JF. Russell-Eggitt IM, et al. Among authors: taylor jf, taylor ds. Br J Ophthalmol. 1989 Apr;73(4):250-4. doi: 10.1136/bjo.73.4.250. Br J Ophthalmol. 1989. PMID: 2713302 Free PMC article.
Implementation of type 1 diabetes genetic risk screening in children in diverse communities: the Virginia PrIMeD project.
Guertin KA, Repaske DR, Taylor JF, Williams ES, Onengut-Gumuscu S, Chen WM, Boggs SR, Yu L, Allen L, Botteon L, Daniel L, Keating KG, Labergerie MK, Lienhart TS, Gonzalez-Mejia JA, Starnowski MJ, Rich SS. Guertin KA, et al. Among authors: taylor jf. Genome Med. 2024 Feb 14;16(1):31. doi: 10.1186/s13073-024-01305-8. Genome Med. 2024. PMID: 38355597 Free PMC article.
509 results