Eyre H - Search Results

1

High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype.

Callen DF, Eyre H, Lane S, Shen Y, Hansmann I, Spinner N, Zackai E, McDonald-McGinn D, Schuffenhauer S, Wauters J, et al. Callen DF, et al. Among authors: eyre h. J Med Genet. 1993 Oct;30(10):828-32. doi: 10.1136/jmg.30.10.828. J Med Genet. 1993. PMID: 8230159 Free PMC article.

2

Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies.

Baker E, Hinton L, Callen DF, Altree M, Dobbie A, Eyre HJ, Sutherland GR, Thompson E, Thompson P, Woollatt E, Haan E. Baker E, et al. Am J Med Genet. 2002 Feb 1;107(4):285-93. doi: 10.1002/ajmg.10159. Am J Med Genet. 2002. PMID: 11840484

3

Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes.

Callen DF, Eyre H, Yip MY, Freemantle J, Haan EA. Callen DF, et al. Among authors: eyre h. Am J Med Genet. 1992 Jul 1;43(4):709-15. doi: 10.1002/ajmg.1320430412. Am J Med Genet. 1992. PMID: 1377870

4

Origins of accessory small ring marker chromosomes derived from chromosome 1.

Callen DF, Eyre H, Fang YY, Guan XY, Veleba A, Martin NJ, McGill J, Haan EA. Callen DF, et al. Among authors: eyre h. J Med Genet. 1999 Nov;36(11):847-53. J Med Genet. 1999. PMID: 10544230 Free PMC article.

5

High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome.

Fang YY, Bain S, Haan EA, Eyre HJ, MacDonald M, Wright TJ, Altherr MR, Riess O, Sutherland G, Callen DF. Fang YY, et al. Among authors: eyre hj. Am J Med Genet. 1997 Sep 5;71(4):453-7. Am J Med Genet. 1997. PMID: 9286454

6

A rare heteromorphism of chromosome 20 and reproductive loss.

Romain DR, Whyte S, Callen DF, Eyre HJ. Romain DR, et al. Among authors: eyre hj. J Med Genet. 1991 Jul;28(7):477-8. doi: 10.1136/jmg.28.7.477. J Med Genet. 1991. PMID: 1895318 Free PMC article.

7

An expanded mouse-human hybrid cell panel for mapping human chromosome 16.

Callen DF, Baker E, Eyre HJ, Lane SA. Callen DF, et al. Among authors: eyre hj. Ann Genet. 1990;33(4):190-5. Ann Genet. 1990. PMID: 2095701

8

A dicentric variant of chromosome 6: characterization by use of in situ hybridisation with the biotinylated probe p308.

Callen DF, Eyre HJ, Ringenbergs ML. Callen DF, et al. Among authors: eyre hj. Clin Genet. 1990 Feb;37(2):81-3. doi: 10.1111/j.1399-0004.1990.tb03483.x. Clin Genet. 1990. PMID: 2311270

9

Mechanisms of small ring formation suggested by the molecular characterization of two small accessory ring chromosomes derived from chromosome 4.

Fang YY, Eyre HJ, Bohlander SK, Estop A, McPherson E, Träger T, Riess O, Callen DF. Fang YY, et al. Among authors: eyre hj. Am J Hum Genet. 1995 Nov;57(5):1137-42. Am J Hum Genet. 1995. PMID: 7485165 Free PMC article.

10

Molecular cytogenetic characterisation of a small ring X chromosome in a Turner patient and in a male patient with congenital abnormalities: role of X inactivation.

Callen DF, Eyre HJ, Dolman G, Garry-Battersby MB, McCreanor JR, Valeba A, McGill JJ. Callen DF, et al. Among authors: eyre hj. J Med Genet. 1995 Feb;32(2):113-6. doi: 10.1136/jmg.32.2.113. J Med Genet. 1995. PMID: 7760319 Free PMC article.

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