Eyre HJ - Search Results

1

Frequency of truly cryptic subtelomere abnormalities--a study of 534 patients and literature review.

Yu S, Baker E, Hinton L, Eyre HJ, Waters W, Higgins S, Sutherland GR, Haan E. Yu S, et al. Among authors: eyre hj. Clin Genet. 2005 Nov;68(5):436-41. doi: 10.1111/j.1399-0004.2005.00513.x. Clin Genet. 2005. PMID: 16207211 Review.

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. Among authors: eyre hj. 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. 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. J Med Genet. 1999 Nov;36(11):847-53. J Med Genet. 1999. PMID: 10544230 Free PMC article.

5

Two unusual G-band variants of the short arm of chromosome 9.

Sutherland GR, Eyre H. Sutherland GR, et al. Clin Genet. 1981 May;19(5):331-4. doi: 10.1111/j.1399-0004.1981.tb00719.x. Clin Genet. 1981. PMID: 7296923 No abstract available.

6

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

7

C16orf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brain.

Bhalla K, Eyre HJ, Whitmore SA, Sutherland GR, Callen DF. Bhalla K, et al. Among authors: eyre hj. J Hum Genet. 1999;44(6):383-7. doi: 10.1007/s100380050183. J Hum Genet. 1999. PMID: 10570909

8

The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridization.

Callen DF, Freemantle CJ, Ringenbergs ML, Baker E, Eyre HJ, Romain D, Haan EA. Callen DF, et al. Among authors: eyre hj. Am J Hum Genet. 1990 Sep;47(3):493-8. Am J Hum Genet. 1990. PMID: 2393023 Free PMC article.

9

The human OTF1 locus which overlaps the CD3Z gene is located at 1q22-->q23.

Sturm RA, Eyre HJ, Baker E, Sutherland GR. Sturm RA, et al. Among authors: eyre hj. Cytogenet Cell Genet. 1995;68(3-4):231-2. doi: 10.1159/000133919. Cytogenet Cell Genet. 1995. PMID: 7842742

10

Detection of microchromosomal aberrations in refractory epilepsy: a pilot study.

McMahon JM, Scheffer IE, Nicholl JK, Waters W, Eyre H, Hinton L, Nelson P, Yu S, Dibbens LM, Berkovic SF, Mulley JC. McMahon JM, et al. Epileptic Disord. 2010 Sep;12(3):192-8. doi: 10.1684/epd.2010.0326. Epub 2010 Jul 19. Epileptic Disord. 2010. PMID: 20643615 Free article.

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