Rajcan-Separovic E - Search Results

1

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

2

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

3

Molecular cytogenetics in reproductive pathology.

Bruyère H, Rajcan-Separovic E, Kalousek DK. Bruyère H, et al. Methods Mol Biol. 2002;204:299-307. doi: 10.1385/1-59259-300-3:299. Methods Mol Biol. 2002. PMID: 12397806

4

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

5

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.

6

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

7

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

8

A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH.

Harvard C, Malenfant P, Koochek M, Creighton S, Mickelson EC, Holden JJ, Lewis ME, Rajcan-Separovic E. Harvard C, et al. Clin Genet. 2005 Apr;67(4):341-51. doi: 10.1111/j.1399-0004.2005.00406.x. Clin Genet. 2005. PMID: 15733271

9

Molecular cytogenetic investigation of two patients with Y chromosome rearrangements and intellectual disability.

Tyson C, Dawson AJ, Bal S, Tomiuk M, Anderson T, Tucker D, Riordan D, Chudoba I, Morash B, Mhanni A, Chudley AE, McGillivray B, Parslow M, Rappold G, Roeth R, Fawcett C, Qiao Y, Harvard C, Rajcan-Separovic E. Tyson C, et al. Am J Med Genet A. 2009 Mar;149A(3):490-5. doi: 10.1002/ajmg.a.32535. Am J Med Genet A. 2009. PMID: 19213034

10

Loss of 1p and 7p in radiation-induced meningiomas identified by comparative genomic hybridization.

Rajcan-Separovic E, Maguire J, Loukianova T, Nisha M, Kalousek D. Rajcan-Separovic E, et al. Cancer Genet Cytogenet. 2003 Jul 1;144(1):6-11. doi: 10.1016/s0165-4608(02)00864-6. Cancer Genet Cytogenet. 2003. PMID: 12810249 Review.

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