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E Rajcan-Separovic

Showing results (11-20 of 24) with videos related to

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Blood|August 9, 2001
Defective hematopoiesis and hepatic steatosis in mice with combined deficiencies of the genes encoding Fancc and Cu/Zn superoxide dismutaseS Hadjur, K Ung, L Wadsworth, et al.
Cytogenetics and Cell Genetics|January 1, 1996
FISH detection of chromosome polymorphism and deletions in the spinal muscular atrophy (SMA) region of 5q13E Rajcan-Separovic, M S Mahadevan, C Lefebvre, et al.
Clinical Genetics|May 24, 2008
Autism-associated familial microdeletion of Xp11.22Y Qiao, X Liu, C Harvard, et al.
Cytogenetic and Genome Research|March 17, 2009
Putatively benign copy number variants in subjects with idiopathic autism spectrum disorder and/or intellectual disabilityY Qiao, C Harvard, N Riendeau, et al.
Clinical Genetics|March 1, 2005
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 CGHC Harvard, P Malenfant, M Koochek, et al.
Human Genetics|June 1, 2010
Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformaticsY Qiao, C Harvard, C Tyson, et al.
Clinical Genetics|January 26, 2006
15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGHM Koochek, C Harvard, M J Hildebrand, et al.
Journal of Medical Genetics|July 24, 2009
Phenomic determinants of genomic variation in autism spectrum disordersY Qiao, N Riendeau, M Koochek, et al.
Human Reproduction (Oxford, England)|September 18, 2010
Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy lossE Rajcan-Separovic, D Diego-Alvarez, W P Robinson, et al.
Journal of Medical Genetics|September 12, 2006
Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1E Rajcan-Separovic, C Harvard, X Liu, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Blood|August 9, 2001
Defective hematopoiesis and hepatic steatosis in mice with combined deficiencies of the genes encoding Fancc and Cu/Zn superoxide dismutaseS Hadjur, K Ung, L Wadsworth, et al.
Cytogenetics and Cell Genetics|January 1, 1996
FISH detection of chromosome polymorphism and deletions in the spinal muscular atrophy (SMA) region of 5q13E Rajcan-Separovic, M S Mahadevan, C Lefebvre, et al.
Clinical Genetics|May 24, 2008
Autism-associated familial microdeletion of Xp11.22Y Qiao, X Liu, C Harvard, et al.
Cytogenetic and Genome Research|March 17, 2009
Putatively benign copy number variants in subjects with idiopathic autism spectrum disorder and/or intellectual disabilityY Qiao, C Harvard, N Riendeau, et al.
Clinical Genetics|March 1, 2005
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 CGHC Harvard, P Malenfant, M Koochek, et al.
Human Genetics|June 1, 2010
Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformaticsY Qiao, C Harvard, C Tyson, et al.
Clinical Genetics|January 26, 2006
15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGHM Koochek, C Harvard, M J Hildebrand, et al.
Journal of Medical Genetics|July 24, 2009
Phenomic determinants of genomic variation in autism spectrum disordersY Qiao, N Riendeau, M Koochek, et al.
Human Reproduction (Oxford, England)|September 18, 2010
Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy lossE Rajcan-Separovic, D Diego-Alvarez, W P Robinson, et al.
Journal of Medical Genetics|September 12, 2006
Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1E Rajcan-Separovic, C Harvard, X Liu, et al.
Pageof 3