Evans HJ - Search Results

1

Association within a family of a balanced autosomal translocation with major mental illness.

St Clair D, Blackwood D, Muir W, Carothers A, Walker M, Spowart G, Gosden C, Evans HJ. St Clair D, et al. Among authors: evans hj. Lancet. 1990 Jul 7;336(8706):13-6. doi: 10.1016/0140-6736(90)91520-k. Lancet. 1990. PMID: 1973210

2

No linkage of chromosome 5q11-q13 markers to schizophrenia in Scottish families.

St Clair D, Blackwood D, Muir W, Baillie D, Hubbard A, Wright A, Evans HJ. St Clair D, et al. Among authors: evans hj. Nature. 1989 May 25;339(6222):305-9. doi: 10.1038/339305a0. Nature. 1989. PMID: 2725644

3

Schizophrenia and chromosomes.

Blackwood DH, Muir WJ, St Clair DM, Evans HJ. Blackwood DH, et al. Among authors: evans hj. Lancet. 1989 Dec 16;2(8677):1459. doi: 10.1016/s0140-6736(89)92071-0. Lancet. 1989. PMID: 2574390 No abstract available.

4

Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindred.

Wright AF, Bhattacharya SS, Aldred MA, Jay M, Carothers AD, Thomas NS, Bird AC, Jay B, Evans HJ. Wright AF, et al. Among authors: evans hj. J Med Genet. 1991 Jul;28(7):453-7. doi: 10.1136/jmg.28.7.453. J Med Genet. 1991. PMID: 1895315 Free PMC article.

5

Heteromorphic X chromosomes in 46,XX males: evidence for the involvement of X-Y interchange.

Evans HJ, Buckton KE, Spowart G, Carothers AD. Evans HJ, et al. Hum Genet. 1979 May 23;49(1):11-31. doi: 10.1007/BF00277683. Hum Genet. 1979. PMID: 572812

6

Linkage heterogeneity and fragile X.

Clayton JF, Gosden CM, Hastie ND, Evans HJ. Clayton JF, et al. Among authors: evans hj. Hum Genet. 1988 Apr;78(4):338-42. doi: 10.1007/BF00291731. Hum Genet. 1988. PMID: 2896154

7

Heterogeneity analysis in 40 X-linked retinitis pigmentosa families.

Teague PW, Aldred MA, Jay M, Dempster M, Harrison C, Carothers AD, Hardwick LJ, Evans HJ, Strain L, Brock DJ, et al. Teague PW, et al. Among authors: evans hj. Am J Hum Genet. 1994 Jul;55(1):105-11. Am J Hum Genet. 1994. PMID: 8023838 Free PMC article.

8

Automation of genetic linkage analysis using fluorescent microsatellite markers.

Mansfield DC, Brown AF, Green DK, Carothers AD, Morris SW, Evans HJ, Wright AF. Mansfield DC, et al. Among authors: evans hj. Genomics. 1994 Nov 15;24(2):225-33. doi: 10.1006/geno.1994.1610. Genomics. 1994. PMID: 7698743

9

Allele loss on short arm of chromosome 17 in breast cancers.

Mackay J, Steel CM, Elder PA, Forrest AP, Evans HJ. Mackay J, et al. Among authors: evans hj. Lancet. 1988 Dec 17;2(8625):1384-5. doi: 10.1016/s0140-6736(88)90584-3. Lancet. 1988. PMID: 2904522

10

Forty four probands with an additional "marker" chromosome.

Buckton KE, Spowart G, Newton MS, Evans HJ. Buckton KE, et al. Among authors: evans hj. Hum Genet. 1985;69(4):353-70. doi: 10.1007/BF00291656. Hum Genet. 1985. PMID: 3857214

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