Flint T - Search Results

1

Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome.

Davies KE, Smith TJ, Bundey S, Read AP, Flint T, Bell M, Speer A. Davies KE, et al. Among authors: flint t. J Med Genet. 1988 Jan;25(1):9-13. doi: 10.1136/jmg.25.1.9. J Med Genet. 1988. PMID: 3162536 Free PMC article.

2

Molecular analysis and diagnosis of Duchenne muscular dystrophy.

Forrest SM, Smith TJ, Cross GS, Kenwrick SJ, England S, Flint T, Davies KE. Forrest SM, et al. Among authors: flint t. J R Coll Physicians Lond. 1988 Apr;22(2):65-7. J R Coll Physicians Lond. 1988. PMID: 3294388 Free PMC article. Review. No abstract available.

3

Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies.

Forrest SM, Cross GS, Flint T, Speer A, Robson KJ, Davies KE. Forrest SM, et al. Among authors: flint t. Genomics. 1988 Feb;2(2):109-14. doi: 10.1016/0888-7543(88)90091-2. Genomics. 1988. PMID: 3410474

4

Deletions of fetal and adult muscle cDNA in Duchenne and Becker muscular dystrophy patients.

Cross GS, Speer A, Rosenthal A, Forrest SM, Smith TJ, Edwards Y, Flint T, Hill D, Davies KE. Cross GS, et al. Among authors: flint t. EMBO J. 1987 Nov;6(11):3277-83. doi: 10.1002/j.1460-2075.1987.tb02646.x. EMBO J. 1987. PMID: 3428261 Free PMC article.

5

Characterization of deletions in the dystrophin gene giving mild phenotypes.

Love DR, Flint TJ, Marsden RF, Bloomfield JF, Daniels RJ, Forrest SM, Gabrielli O, Giorgi P, Novelli G, Davies KE. Love DR, et al. Among authors: flint tj. Am J Med Genet. 1990 Sep;37(1):136-42. doi: 10.1002/ajmg.1320370132. Am J Med Genet. 1990. PMID: 2240031

6

Genotype prediction in the fragile X syndrome.

Hirst MC, Nakahori Y, Knight SJ, Schwartz C, Thibodeau SN, Roche A, Flint TJ, Connor JM, Fryns JP, Davies KE. Hirst MC, et al. Among authors: flint tj. J Med Genet. 1991 Dec;28(12):824-9. doi: 10.1136/jmg.28.12.824. J Med Genet. 1991. PMID: 1757957 Free PMC article.

7

Becker muscular dystrophy patient with a large intragenic dystrophin deletion: implications for functional minigenes and gene therapy.

Love DR, Flint TJ, Genet SA, Middleton-Price HR, Davies KE. Love DR, et al. Among authors: flint tj. J Med Genet. 1991 Dec;28(12):860-4. doi: 10.1136/jmg.28.12.860. J Med Genet. 1991. PMID: 1757963 Free PMC article.

8

Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115.

Passos-Bueno MR, Rapaport D, Love D, Flint T, Bortolini ER, Zatz M, Davies KE. Passos-Bueno MR, et al. Among authors: flint t. J Med Genet. 1990 Mar;27(3):145-50. doi: 10.1136/jmg.27.3.145. J Med Genet. 1990. PMID: 2182872 Free PMC article.

9

Molecular analysis of Duchenne and Becker muscular dystrophies.

Love DR, Forrest SM, Smith TJ, England S, Flint T, Davies KE, Speer A. Love DR, et al. Among authors: flint t. Br Med Bull. 1989 Jul;45(3):659-80. doi: 10.1093/oxfordjournals.bmb.a072351. Br Med Bull. 1989. PMID: 2688822 Review.

10

Genetic and physical mapping of a novel region close to the fragile X site on the human X chromosome.

Patterson MN, Bell MV, Bloomfield J, Flint T, Dorkins H, Thibodeau SN, Schaid D, Bren G, Schwartz CE, Wieringa B, et al. Patterson MN, et al. Among authors: flint t. Genomics. 1989 May;4(4):570-8. doi: 10.1016/0888-7543(89)90281-4. Genomics. 1989. PMID: 2744766

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