Mountford RC - Search Results

1

DNA probes in differential diagnosis of Becker muscular dystrophy and spinal muscular atrophy.

Lunt PW, Cumming WJ, Kingston H, Read AP, Mountford RC, Mahon M, Harris R. Lunt PW, et al. Among authors: mountford rc. Lancet. 1989 Jan 7;1(8628):46-7. doi: 10.1016/s0140-6736(89)91704-2. Lancet. 1989. PMID: 2563028 No abstract available.

2

Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophy.

Forrest SM, Smith TJ, Cross GS, Read AP, Thomas NS, Mountford RC, Harper PS, Geirsson RT, Davies KE. Forrest SM, et al. Among authors: mountford rc. Lancet. 1987 Dec 5;2(8571):1294-7. doi: 10.1016/s0140-6736(87)91192-5. Lancet. 1987. PMID: 2890901

3

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: mountford rc. Hum Genet. 1988 Oct;80(2):152-6. doi: 10.1007/BF00702859. Hum Genet. 1988. PMID: 3169738

4

A register based system for gene tracking in Duchenne muscular dystrophy.

Read AP, Kerzin-Storrar L, Mountford RC, Elles RG, Harris R. Read AP, et al. Among authors: mountford rc. J Med Genet. 1986 Dec;23(6):581-6. doi: 10.1136/jmg.23.6.581. J Med Genet. 1986. PMID: 2879930 Free PMC article.

5

Norrie disease resulting from a gene deletion: clinical features and DNA studies.

Donnai D, Mountford RC, Read AP. Donnai D, et al. Among authors: mountford rc. J Med Genet. 1988 Feb;25(2):73-8. doi: 10.1136/jmg.25.2.73. J Med Genet. 1988. PMID: 3162283 Free PMC article.

6

A BanI RFLP at a deletion hotspot in the human dystrophin gene.

Read AP, Mountford R. Read AP, et al. Nucleic Acids Res. 1990 Jan 25;18(2):385. doi: 10.1093/nar/18.2.385. Nucleic Acids Res. 1990. PMID: 1970164 Free PMC article.

7

Molecular diagnosis of spinal muscular atrophy.

Stewart H, Wallace A, McGaughran J, Mountford R, Kingston H. Stewart H, et al. Arch Dis Child. 1998 Jun;78(6):531-5. doi: 10.1136/adc.78.6.531. Arch Dis Child. 1998. PMID: 9713008 Free PMC article.

8

Molecular genetics in the National Health Service in Britain.

Harris R, Elles R, Craufurd D, Dodge A, Ivinson A, Hodgkinson K, Mountford R, Schwartz M, Strachan T, Read A. Harris R, et al. J Med Genet. 1989 Apr;26(4):219-25. doi: 10.1136/jmg.26.4.219. J Med Genet. 1989. PMID: 2523972 Free PMC article.

9

Occurrence of Duchenne dystrophy in Klinefelter's syndrome.

Ramesh V, Mountford R, Kingston HM, Kelsey A, Noronha MJ, Clarke MA. Ramesh V, et al. Arch Dis Child. 1993 Oct;69(4):453-4. doi: 10.1136/adc.69.4.453. Arch Dis Child. 1993. PMID: 8259881 Free PMC article.

10

Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysis.

Read AP, Thakker RV, Davies KE, Mountford RC, Brenton DP, Davies M, Glorieux F, Harris R, Hendy GN, King A, et al. Read AP, et al. Among authors: mountford rc. Hum Genet. 1986 Jul;73(3):267-70. doi: 10.1007/BF00401242. Hum Genet. 1986. PMID: 3015770

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