Rajcan-Separovic E - Search Results

1

Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation.

Friedman JM, Baross A, Delaney AD, Ally A, Arbour L, Armstrong L, Asano J, Bailey DK, Barber S, Birch P, Brown-John M, Cao M, Chan S, Charest DL, Farnoud N, Fernandes N, Flibotte S, Go A, Gibson WT, Holt RA, Jones SJ, Kennedy GC, Krzywinski M, Langlois S, Li HI, McGillivray BC, Nayar T, Pugh TJ, Rajcan-Separovic E, Schein JE, Schnerch A, Siddiqui A, Van Allen MI, Wilson G, Yong SL, Zahir F, Eydoux P, Marra MA. Friedman JM, et al. Am J Hum Genet. 2006 Sep;79(3):500-13. doi: 10.1086/507471. Epub 2006 Jul 25. Am J Hum Genet. 2006. PMID: 16909388 Free PMC article.

2

Elucidation of a cryptic interstitial 7q31.3 deletion in a patient with a language disorder and mild mental retardation by array-CGH.

Tyson C, McGillivray B, Chijiwa C, Rajcan-Separovic E. Tyson C, et al. Am J Med Genet A. 2004 Sep 1;129A(3):254-60. doi: 10.1002/ajmg.a.30245. Am J Med Genet A. 2004. PMID: 15326624

3

Submicroscopic deletions and duplications in individuals with intellectual disability detected by array-CGH.

Tyson C, Harvard C, Locker R, Friedman JM, Langlois S, Lewis ME, Van Allen M, Somerville M, Arbour L, Clarke L, McGilivray B, Yong SL, Siegel-Bartel J, Rajcan-Separovic E. Tyson C, et al. Am J Med Genet A. 2005 Dec 15;139(3):173-85. doi: 10.1002/ajmg.a.31015. Am J Med Genet A. 2005. PMID: 16283669

4

Phenotype-genotype characterization of alpha-thalassemia mental retardation syndrome due to isolated monosomy of 16p13.3.

Gibson WT, Harvard C, Qiao Y, Somerville MJ, Lewis ME, Rajcan-Separovic E. Gibson WT, et al. Am J Med Genet A. 2008 Jan 15;146A(2):225-32. doi: 10.1002/ajmg.a.32056. Am J Med Genet A. 2008. PMID: 18076105

5

Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH.

Tyson C, Qiao Y, Harvard C, Liu X, Bernier FP, McGillivray B, Farrell SA, Arbour L, Chudley AE, Clarke L, Gibson W, Dyack S, McLeod R, Costa T, Vanallen MI, Yong SL, Graham GE, Macleod P, Patel MS, Hurlburt J, Holden JJ, Lewis SM, Rajcan-Separovic E. Tyson C, et al. Mol Cytogenet. 2008 Nov 11;1:23. doi: 10.1186/1755-8166-1-23. Mol Cytogenet. 2008. PMID: 19000322 Free PMC article.

6

Familial cryptic translocation (2;17) ascertained through recurrent spontaneous abortions.

Bruyere H, Rajcan-Separovic E, Doyle J, Pantzar T, Langlois S. Bruyere H, et al. Am J Med Genet A. 2003 Dec 15;123A(3):285-9. doi: 10.1002/ajmg.a.20228. Am J Med Genet A. 2003. PMID: 14608651

7

15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.

Koochek M, Harvard C, Hildebrand MJ, Van Allen M, Wingert H, Mickelson E, Holden JJ, Rajcan-Separovic E, Lewis ME. Koochek M, et al. Clin Genet. 2006 Feb;69(2):124-34. doi: 10.1111/j.1399-0004.2005.00560.x. Clin Genet. 2006. PMID: 16433693

8

Copy number variants (CNVs) analysis in a deeply phenotyped cohort of individuals with intellectual disability (ID).

Qiao Y, Mercier E, Dastan J, Hurlburt J, McGillivray B, Chudley AE, Farrell S, Bernier FP, Lewis MS, Pavlidis P, Rajcan-Separovic E. Qiao Y, et al. BMC Med Genet. 2014 Jul 16;15:82. doi: 10.1186/1471-2350-15-82. BMC Med Genet. 2014. PMID: 25030379 Free PMC article.

9

Recurrent trisomy 15 in a female carrier of der(15)t(Y;15)(q12;p13).

Rajcan-Separovic E, Robinson WP, Stephenson M, Pantzar T, Arbour L, McFadden D, Guscott J. Rajcan-Separovic E, et al. Am J Med Genet. 2001 Apr 1;99(4):320-4. doi: 10.1002/1096-8628(2001)9999:9999<::aid-ajmg1173>3.0.co;2-1. Am J Med Genet. 2001. PMID: 11252000

10

Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformatics.

Qiao Y, Harvard C, Tyson C, Liu X, Fawcett C, Pavlidis P, Holden JJ, Lewis ME, Rajcan-Separovic E. Qiao Y, et al. Hum Genet. 2010 Aug;128(2):179-94. doi: 10.1007/s00439-010-0837-0. Epub 2010 May 29. Hum Genet. 2010. PMID: 20512354

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