Old JM - Search Results

1

Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families.

Dorkins H, Junien C, Mandel JL, Wrogemann K, Moison JP, Martinez M, Old JM, Bundey S, Schwartz M, Carpenter N, et al. Dorkins H, et al. Among authors: old jm. Hum Genet. 1985;71(2):103-7. doi: 10.1007/BF00283362. Hum Genet. 1985. PMID: 2995231

2

Detection and exclusion of carriers of ornithine transcarbamylase deficiency by RFLP analysis.

Schwartz M, Christensen E, Christensen NC, Skovby F, Davies KE, Old JM. Schwartz M, et al. Among authors: old jm. Clin Genet. 1986 May;29(5):449-52. doi: 10.1111/j.1399-0004.1986.tb00520.x. Clin Genet. 1986. PMID: 3017613

3

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: old jm. Ann Clin Res. 1986;18(5-6):231-3. Ann Clin Res. 1986. PMID: 2882726 No abstract available.

4

Prenatal diagnosis of Duchenne muscular dystrophy by DNA analysis.

Old JM, Davies KE. Old JM, et al. J Med Genet. 1986 Dec;23(6):556-9. doi: 10.1136/jmg.23.6.556. J Med Genet. 1986. PMID: 2879927 Free PMC article.

5

Meiotic recombination between two polymorphic restriction sites within the beta globin gene cluster.

Old JM, Heath C, Fitches A, Thein SL, Jeffreys AJ, Petrou M, Modell B, Weatherall DJ. Old JM, et al. J Med Genet. 1986 Feb;23(1):14-8. doi: 10.1136/jmg.23.1.14. J Med Genet. 1986. PMID: 3005579 Free PMC article.

6

Evidence linking familial thrombosis with a defective antithrombin III gene in two British kindreds.

Sacks SH, Old JM, Reeders ST, Weatherall DJ, Douglas AS, Winter JH, Rizza CR. Sacks SH, et al. Among authors: old jm. J Med Genet. 1988 Jan;25(1):20-4. doi: 10.1136/jmg.25.1.20. J Med Genet. 1988. PMID: 3162535 Free PMC article.

7

Analysis of beta-globin gene haplotypes in Asian Indians: origin and spread of beta-thalassaemia on the Indian subcontinent.

Varawalla NY, Fitches AC, Old JM. Varawalla NY, et al. Among authors: old jm. Hum Genet. 1992 Dec;90(4):443-9. doi: 10.1007/BF00220475. Hum Genet. 1992. PMID: 1362388

8

Prenatal diagnosis of the common haemoglobin disorders.

Weatherall DJ, Old JM, Thein SL, Wainscoat JS, Clegg JB. Weatherall DJ, et al. Among authors: old jm. J Med Genet. 1985 Dec;22(6):422-30. doi: 10.1136/jmg.22.6.422. J Med Genet. 1985. PMID: 3001310 Free PMC article. Review.

9

Prenatal exclusion of ornithine transcarbamylase deficiency by direct gene analysis.

Old JM, Briand PL, Purvis-Smith S, Howard NJ, Wilcken B, Hammond J, Pearson P, Cathelineau L, Williamson R, Davies KE. Old JM, et al. Lancet. 1985 Jan 12;1(8420):73-5. doi: 10.1016/s0140-6736(85)91966-x. Lancet. 1985. PMID: 2857026

10

Carrier testing strategy in haemophilia A.

Janco RL, Phillips JA 3rd, Orlando P, Davies KE, Old J, Antonarakis SE. Janco RL, et al. Lancet. 1986 Jan 18;1(8473):148-9. doi: 10.1016/s0140-6736(86)92279-8. Lancet. 1986. PMID: 2867360 Clinical Trial. No abstract available.

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