Flint T - Search Results

1

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

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

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.

5

Molecular heterogeneity of the fragile X syndrome.

Nakahori Y, Knight SJ, Holland J, Schwartz C, Roche A, Tarleton J, Wong S, Flint TJ, Froster-Iskenius U, Bentley D, et al. Nakahori Y, et al. Among authors: flint tj. Nucleic Acids Res. 1991 Aug 25;19(16):4355-9. doi: 10.1093/nar/19.16.4355. Nucleic Acids Res. 1991. PMID: 1886762 Free PMC article.

6

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.

7

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

8

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

9

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

10

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. Among authors: flint t. Genomics. 1990 Oct;8(2):189-93. doi: 10.1016/0888-7543(90)90271-u. Genomics. 1990. PMID: 1979046

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

83 results

Search Page

Filters