Slater HR - Search Results

1

High-resolution identification of chromosomal abnormalities using oligonucleotide arrays containing 116,204 SNPs.

Slater HR, Bailey DK, Ren H, Cao M, Bell K, Nasioulas S, Henke R, Choo KH, Kennedy GC. Slater HR, et al. Am J Hum Genet. 2005 Nov;77(5):709-26. doi: 10.1086/497343. Epub 2005 Sep 16. Am J Hum Genet. 2005. PMID: 16252233 Free PMC article.

2

BAC-based PCR fragment microarray: high-resolution detection of chromosomal deletion and duplication breakpoints.

Ren H, Francis W, Boys A, Chueh AC, Wong N, La P, Wong LH, Ryan J, Slater HR, Choo KH. Ren H, et al. Among authors: slater hr. Hum Mutat. 2005 May;25(5):476-82. doi: 10.1002/humu.20164. Hum Mutat. 2005. PMID: 15832308

3

Detection of cryptic subtelomeric chromosome abnormalities and identification of anonymous chromatin using a quantitative multiplex ligation-dependent probe amplification (MLPA) assay.

Northrop EL, Ren H, Bruno DL, McGhie JD, Coffa J, Schouten J, Choo KH, Slater HR. Northrop EL, et al. Among authors: slater hr. Hum Mutat. 2005 Nov;26(5):477-86. doi: 10.1002/humu.20243. Hum Mutat. 2005. PMID: 16170807

4

Improved testing for CMT1A and HNPP using multiplex ligation-dependent probe amplification (MLPA) with rapid DNA preparations: comparison with the interphase FISH method.

Slater H, Bruno D, Ren H, La P, Burgess T, Hills L, Nouri S, Schouten J, Choo KH. Slater H, et al. Hum Mutat. 2004 Aug;24(2):164-71. doi: 10.1002/humu.20072. Hum Mutat. 2004. PMID: 15241798

5

Centric fission--simple and complex mechanisms.

Perry J, Slater HR, Choo KH. Perry J, et al. Among authors: slater hr. Chromosome Res. 2004;12(6):627-40. doi: 10.1023/B:CHRO.0000036594.38997.59. Chromosome Res. 2004. PMID: 15289668 Review.

6

Molecular distinction between true centric fission and pericentric duplication-fission.

Perry J, Nouri S, La P, Daniel A, Wu Z, Purvis-Smith S, Northrop E, Choo KH, Slater HR. Perry J, et al. Among authors: slater hr. Hum Genet. 2005 Mar;116(4):300-10. doi: 10.1007/s00439-004-1209-4. Epub 2005 Jan 27. Hum Genet. 2005. PMID: 15712016

7

Analysis of SNP content of 82 common copy-number polymorphisms from the Database of Genomic Variations.

Slater HR, Bailey DK, Ren H, Cao M, Bell K, Nasioulas S, Henke R, Choo KH, Kennedy GC. Slater HR, et al. Am J Hum Genet. 2006 Apr;78(4):730-1. doi: 10.1086/502683. Am J Hum Genet. 2006. PMID: 16532405 Free PMC article. No abstract available.

8

A functional marker centromere with no detectable alpha-satellite, satellite III, or CENP-B protein: activation of a latent centromere?

Voullaire LE, Slater HR, Petrovic V, Choo KH. Voullaire LE, et al. Among authors: slater hr. Am J Hum Genet. 1993 Jun;52(6):1153-63. Am J Hum Genet. 1993. PMID: 7684888 Free PMC article.

9

Confirmation of trisomy 22 in two cases using chromosome painting: comparison with t(11;22).

Slater HR, Voullaire LE, Vaux CE, Bankier A, Pertile M, Choo KH. Slater HR, et al. Am J Med Genet. 1993 Jun 1;46(4):434-7. doi: 10.1002/ajmg.1320460417. Am J Med Genet. 1993. PMID: 8357017

10

Neocentromere formation in a stable ring 1p32-p36.1 chromosome.

Slater HR, Nouri S, Earle E, Lo AW, Hale LG, Choo KH. Slater HR, et al. J Med Genet. 1999 Dec;36(12):914-8. J Med Genet. 1999. PMID: 10593999 Free PMC article.

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