Holloway S - Search Results

1

A chromosomal duplication map of malformations: regions of suspected haplo- and triplolethality--and tolerance of segmental aneuploidy--in humans.

Brewer C, Holloway S, Zawalnyski P, Schinzel A, FitzPatrick D. Brewer C, et al. Among authors: holloway s. Am J Hum Genet. 1999 Jun;64(6):1702-8. doi: 10.1086/302410. Am J Hum Genet. 1999. PMID: 10330358 Free PMC article.

2

Coefficients of relationship by isonymy among the parents of Scottish twins: a test of familial aggregation.

Holloway SM, Sofaer JA. Holloway SM, et al. Hum Biol. 1990 Jun;62(3):429-35. Hum Biol. 1990. PMID: 2373512

3

Attitudes of general practitioners to presymptomatic testing for Huntington's disease.

Mennie ME, Holloway SM, Brock DJ. Mennie ME, et al. Among authors: holloway sm. J Med Genet. 1990 Apr;27(4):224-7. doi: 10.1136/jmg.27.4.224. J Med Genet. 1990. PMID: 2139128 Free PMC article.

4

Long-term attendance at follow-up of women assessed as being at increased risk of developing breast cancer in south-east Scotland.

Holloway S, Porteous M, Cetnarskyj R, Anderson E, Campbell J, Steel M, Campbell H. Holloway S, et al. Community Genet. 2007;10(4):252-60. doi: 10.1159/000106564. Community Genet. 2007. PMID: 17895631

5

Uptake of testing for BRCA1/2 mutations in South East Scotland.

Holloway SM, Bernhard B, Campbell H, Lam WW. Holloway SM, et al. Eur J Hum Genet. 2008 Aug;16(8):906-12. doi: 10.1038/ejhg.2008.17. Epub 2008 Feb 20. Eur J Hum Genet. 2008. PMID: 18285832

6

A novel acropectoral syndrome maps to chromosome 7q36.

Dundar M, Gordon TM, Ozyazgan I, Oguzkaya F, Ozkul Y, Cooke A, Wilkinson AG, Holloway S, Goodman FR, Tolmie JL. Dundar M, et al. Among authors: holloway s. J Med Genet. 2001 May;38(5):304-9. doi: 10.1136/jmg.38.5.304. J Med Genet. 2001. PMID: 11333865 Free PMC article.

7

The incidence of cystic fibrosis in Scotland calculated from heterozygote frequencies.

Brock DJ, Gilfillan A, Holloway S. Brock DJ, et al. Among authors: holloway s. Clin Genet. 1998 Jan;53(1):47-9. doi: 10.1034/j.1399-0004.1998.531530109.x. Clin Genet. 1998. PMID: 9550361

8

Use of linkage disequilibrium data in prenatal diagnosis of cystic fibrosis.

Strain L, Curtis A, Mennie M, Holloway S, Brock DJ. Strain L, et al. Among authors: holloway s. Hum Genet. 1988 Sep;80(1):75-7. doi: 10.1007/BF00451460. Hum Genet. 1988. PMID: 3417307

9

Risks of fetal cystic fibrosis based on linkage disequilibrium data.

Holloway S, Brock DJ. Holloway S, et al. Hum Genet. 1989 Aug;83(1):52-4. doi: 10.1007/BF00274147. Hum Genet. 1989. PMID: 2570017

10

Prenatal exclusion testing for Huntington's disease: a problem of too much information.

Millan FA, Curtis A, Mennie M, Holloway S, Boxer M, Faed MJ, Crawford JW, Liston WA, Brock DJ. Millan FA, et al. Among authors: holloway s. J Med Genet. 1989 Feb;26(2):83-5. doi: 10.1136/jmg.26.2.83. J Med Genet. 1989. PMID: 2563777 Free PMC article.

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