Kenwrick S - Search Results

1

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: kenwrick s. Genomics. 1987 Sep;1(1):43-51. doi: 10.1016/0888-7543(87)90103-0. Genomics. 1987. PMID: 2889661

2

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. Among authors: kenwrick s. 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.

3

Physical mapping distal to the DMD locus.

Love DR, Bloomfield JF, Kenwrick SJ, Yates JR, Davies KE. Love DR, et al. Among authors: kenwrick sj. Genomics. 1990 Sep;8(1):106-12. doi: 10.1016/0888-7543(90)90231-i. Genomics. 1990. PMID: 2081587

4

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: kenwrick s. Muscle Nerve. 1987 Mar-Apr;10(3):191-9. doi: 10.1002/mus.880100302. Muscle Nerve. 1987. PMID: 2882417 Review.

5

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. Cell. 1987 Jan 30;48(2):351-7. doi: 10.1016/0092-8674(87)90438-7. Cell. 1987. PMID: 3026644

6

Patterns of exon deletions in Duchenne and Becker muscular dystrophy.

Read AP, Mountford RC, Forrest SM, Kenwrick SJ, Davies KE, Harris R. Read AP, et al. Among authors: kenwrick sj. Hum Genet. 1988 Oct;80(2):152-6. doi: 10.1007/BF00702859. Hum Genet. 1988. PMID: 3169738

7

The molecular genetics of human monogenic diseases.

Ball SP, Kenwrick SJ, Davies KE. Ball SP, et al. Among authors: kenwrick sj. Biotechnol Genet Eng Rev. 1985;3:275-309. doi: 10.1080/02648725.1985.10647816. Biotechnol Genet Eng Rev. 1985. PMID: 3004535 Review. No abstract available.

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: kenwrick sj. Am J Med Genet. 1988 Mar;29(3):557-64. doi: 10.1002/ajmg.1320290313. Am J Med Genet. 1988. PMID: 2837087

9

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: kenwrick sj. J Muscle Res Cell Motil. 1988 Feb;9(1):1-8. doi: 10.1007/BF01682143. J Muscle Res Cell Motil. 1988. PMID: 3292577 Review.

10

Localisation of the endpoints of deletions in the 5' region of the Duchenne gene using a sequence isolated by chromosome jumping.

Kenwrick SJ, Smith TJ, England S, Collins F, Davies KE. Kenwrick SJ, et al. Nucleic Acids Res. 1988 Feb 25;16(4):1305-17. doi: 10.1093/nar/16.4.1305. Nucleic Acids Res. 1988. PMID: 3347492 Free PMC article.

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