Patterson M - Search Results

1

Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresis.

Kenwrick S, Patterson M, Speer A, Fischbeck K, Davies K. Kenwrick S, et al. Among authors: patterson m. Cell. 1987 Jan 30;48(2):351-7. doi: 10.1016/0092-8674(87)90438-7. Cell. 1987. PMID: 3026644

2

Molecular analysis of muscular dystrophy.

Davies KE, Kenwrick SJ, Patterson MN, Smith TJ, Forrest SM, Dorkins HR, Cross GS, England SB. Davies KE, et al. Among authors: patterson mn. J Muscle Res Cell Motil. 1988 Feb;9(1):1-8. doi: 10.1007/BF01682143. J Muscle Res Cell Motil. 1988. PMID: 3292577 Review.

3

Molecular analysis of human muscular dystrophies.

Davies KE, Forrest S, Smith T, Kenwrick S, Ball S, Dorkins H, Patterson M. Davies KE, et al. Among authors: patterson m. Muscle Nerve. 1987 Mar-Apr;10(3):191-9. doi: 10.1002/mus.880100302. Muscle Nerve. 1987. PMID: 2882417 Review.

4

Molecular analysis of X-linked diseases.

Davies KE, Ball SP, Dorkins HR, Forrest SM, Kenwrick SJ, Patterson MN, Smith TJ, Old JM, King AW, Thakker RV, et al. Davies KE, et al. Among authors: patterson mn. Ann Clin Res. 1986;18(5-6):231-3. Ann Clin Res. 1986. PMID: 2882726 No abstract available.

5

Molecular analysis of human X-linked diseases.

Davies KE, Ball SP, Dorkins HR, Forrest SM, Kenwrick SJ, King AW, Lavenir IJ, McGlade SA, Patterson MN, Smith TJ, et al. Davies KE, et al. Among authors: patterson mn. Cold Spring Harb Symp Quant Biol. 1986;51 Pt 1:337-43. doi: 10.1101/sqb.1986.051.01.039. Cold Spring Harb Symp Quant Biol. 1986. PMID: 3472730 No abstract available.

6

Chromosome-specific alpha satellite DNA from human chromosome 1: hierarchical structure and genomic organization of a polymorphic domain spanning several hundred kilobase pairs of centromeric DNA.

Waye JS, Durfy SJ, Pinkel D, Kenwrick S, Patterson M, Davies KE, Willard HF. Waye JS, et al. Among authors: patterson m. Genomics. 1987 Sep;1(1):43-51. doi: 10.1016/0888-7543(87)90103-0. Genomics. 1987. PMID: 2889661

7

Pulsed-field gel mapping studies in the vicinity of the fragile site at Xq27.3.

Patterson M, Bell M, Schwartz C, Davies K. Patterson M, et al. Am J Med Genet. 1988 May-Jun;30(1-2):581-91. doi: 10.1002/ajmg.1320300159. Am J Med Genet. 1988. PMID: 3177471

8

Fine mapping of glycerol kinase deficiency and congenital adrenal hypoplasia within Xp21 on the short arm of the human X chromosome.

Davies KE, Patterson MN, Kenwrick SJ, Bell MV, Sloan HR, Westman JA, Elsas LJ 2nd, Mahan J. Davies KE, et al. Among authors: patterson mn. Am J Med Genet. 1988 Mar;29(3):557-64. doi: 10.1002/ajmg.1320290313. Am J Med Genet. 1988. PMID: 2837087

9

Mapping of DNA markers close to the fragile site on the human X chromosome at Xq27.3.

Patterson M, Kenwrick S, Thibodeau S, Faulk K, Mattei MG, Mattei JF, Davies KE. Patterson M, et al. Nucleic Acids Res. 1987 Mar 25;15(6):2639-51. doi: 10.1093/nar/15.6.2639. Nucleic Acids Res. 1987. PMID: 2882476 Free PMC article.

10

Physical mapping studies on the human X chromosome in the region Xq27-Xqter.

Patterson M, Schwartz C, Bell M, Sauer S, Hofker M, Trask B, van den Engh G, Davies KE. Patterson M, et al. Genomics. 1987 Dec;1(4):297-306. doi: 10.1016/0888-7543(87)90028-0. Genomics. 1987. PMID: 3482420

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

1,963 results

Search Page