Flint TJ - Search Results

1

Linkage analysis of spinal muscular atrophy.

Daniels RJ, Thomas NH, MacKinnon RN, Lehner T, Ott J, Flint TJ, Dubowitz V, Ignatius J, Donner M, Zerres K, et al. Daniels RJ, et al. Among authors: flint tj. Genomics. 1992 Feb;12(2):335-9. doi: 10.1016/0888-7543(92)90382-3. Genomics. 1992. PMID: 1346777

2

Linear order of new and established DNA markers around the fragile site at Xq27.3.

Hirst MC, Roche A, Flint TJ, MacKinnon RN, Bassett JH, Nakahori Y, Watson JE, Bell MV, Patterson MN, Boyd Y, et al. Hirst MC, et al. Among authors: flint tj. Genomics. 1991 May;10(1):243-9. doi: 10.1016/0888-7543(91)90506-a. Genomics. 1991. PMID: 2045104

3

Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome.

Bell MV, Hirst MC, Nakahori Y, MacKinnon RN, Roche A, Flint TJ, Jacobs PA, Tommerup N, Tranebjaerg L, Froster-Iskenius U, et al. Bell MV, et al. Among authors: flint tj. Cell. 1991 Feb 22;64(4):861-6. doi: 10.1016/0092-8674(91)90514-y. Cell. 1991. PMID: 1997211

4

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

5

No genetic linkage detected for schizophrenia to Xq27-q28.

Delisi LE, Crow TJ, Davies KE, Terwilliger JD, Ott J, Ram R, Flint T, Boccio A. Delisi LE, et al. Among authors: flint t. Br J Psychiatry. 1991 May;158:630-4. doi: 10.1192/bjp.158.5.630. Br J Psychiatry. 1991. PMID: 1677599

6

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. Genomics. 1988 Feb;2(2):109-14. doi: 10.1016/0888-7543(88)90091-2. Genomics. 1988. PMID: 3410474

7

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. Genomics. 1989 May;4(4):570-8. doi: 10.1016/0888-7543(89)90281-4. Genomics. 1989. PMID: 2744766

8

Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families.

Thakker RV, Davies KE, Read AP, Tippett P, Wooding C, Flint T, Wood S, Kruse TA, Whyte MP, O'Riordan JL. Thakker RV, et al. Genomics. 1990 Oct;8(2):189-93. doi: 10.1016/0888-7543(90)90271-u. Genomics. 1990. PMID: 1979046

9

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.

10

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.

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