Warburton PE - Search Results

1

Identification of a neocentromere in a rearranged Y chromosome with no detectable DYZ3 centromeric sequence.

Assumpção JG, Berkofsky-Fessler W, Viguetti Campos N, Trevas Maciel-Guerra A, Li S, Melaragno MI, Palandi de Mello M, Warburton PE. Assumpção JG, et al. Among authors: warburton pe. Am J Med Genet. 2002 Dec 1;113(3):263-7. doi: 10.1002/ajmg.10701. Am J Med Genet. 2002. PMID: 12439894

2

Chromosome 13q neocentromeres: molecular cytogenetic characterization of three additional cases and clinical spectrum.

Li S, Malafiej P, Levy B, Mahmood R, Field M, Hughes T, Lockhart LH, Wu Z, Huang M, Hirschhorn K, Velagaleti GV, Daniel A, Warburton PE. Li S, et al. Among authors: warburton pe. Am J Med Genet. 2002 Jul 1;110(3):258-67. doi: 10.1002/ajmg.10454. Am J Med Genet. 2002. PMID: 12116235

3

Genomic microarray analysis reveals distinct locations for the CENP-A binding domains in three human chromosome 13q32 neocentromeres.

Alonso A, Mahmood R, Li S, Cheung F, Yoda K, Warburton PE. Alonso A, et al. Among authors: warburton pe. Hum Mol Genet. 2003 Oct 15;12(20):2711-21. doi: 10.1093/hmg/ddg282. Epub 2003 Aug 19. Hum Mol Genet. 2003. PMID: 12928482

4

Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere.

Warburton PE, Dolled M, Mahmood R, Alonso A, Li S, Naritomi K, Tohma T, Nagai T, Hasegawa T, Ohashi H, Govaerts LC, Eussen BH, Van Hemel JO, Lozzio C, Schwartz S, Dowhanick-Morrissette JJ, Spinner NB, Rivera H, Crolla JA, Yu C, Warburton D. Warburton PE, et al. Among authors: warburton d. Am J Hum Genet. 2000 Jun;66(6):1794-806. doi: 10.1086/302924. Epub 2000 Apr 24. Am J Hum Genet. 2000. PMID: 10777715 Free PMC article. Review.

5

Prenatal diagnosis of a karyotypically normal pregnancy in a mother with a supernumerary neocentric 13q21 -->13q22 chromosome and balancing reciprocal deletion.

Knegt AC, Li S, Engelen JJ, Bijlsma EK, Warburton PE. Knegt AC, et al. Among authors: warburton pe. Prenat Diagn. 2003 Mar;23(3):215-20. doi: 10.1002/pd.559. Prenat Diagn. 2003. PMID: 12627422

6

Transmission of a fully functional human neocentromere through three generations.

Tyler-Smith C, Gimelli G, Giglio S, Floridia G, Pandya A, Terzoli G, Warburton PE, Earnshaw WC, Zuffardi O. Tyler-Smith C, et al. Among authors: warburton pe. Am J Hum Genet. 1999 May;64(5):1440-4. doi: 10.1086/302380. Am J Hum Genet. 1999. PMID: 10205277 Free PMC article.

7

Unique case of mosaicism involving two morphologically similar marker chromosomes of different centric origin in a patient with developmental delay.

Levy B, Jalal SM, Dunn TM, Warburton PE, Tonk VS, Hirschhorn K, Lockhart LH, Hughes T, Velagaleti GV. Levy B, et al. Among authors: warburton pe. Am J Med Genet. 2002 Mar 15;108(3):198-204. doi: 10.1002/ajmg.10263. Am J Med Genet. 2002. PMID: 11891685

8

Human CENP-H multimers colocalize with CENP-A and CENP-C at active centromere--kinetochore complexes.

Sugata N, Li S, Earnshaw WC, Yen TJ, Yoda K, Masumoto H, Munekata E, Warburton PE, Todokoro K. Sugata N, et al. Among authors: warburton pe. Hum Mol Genet. 2000 Nov 22;9(19):2919-26. doi: 10.1093/hmg/9.19.2919. Hum Mol Genet. 2000. PMID: 11092768

9

Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome.

Levy B, Papenhausen P, Tepperberg J, Dunn T, Fallet S, Magid M, Kardon N, Hirschhorn K, Warburton P. Levy B, et al. Cytogenet Cell Genet. 2000;91(1-4):165-70. doi: 10.1159/000056839. Cytogenet Cell Genet. 2000. PMID: 11173851

10

An unstable dicentric Robertsonian translocation in a markedly discordant twin.

Lebo RV, Wyandt HE, Warburton PE, Li S, Milunsky JM. Lebo RV, et al. Among authors: warburton pe. Clin Genet. 2002 Nov;62(5):383-9. doi: 10.1034/j.1399-0004.2002.620505.x. Clin Genet. 2002. PMID: 12431253

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