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J Schoumans

Showing results (1-10 of 23) with videos related to

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Cytogenetic and Genome Research|November 17, 2011
Interpretation of array comparative genome hybridization data: a major challengeA C J Gijsbers, J Schoumans, C A L Ruivenkamp
British Journal of Haematology|September 21, 2001
Interphase fluorescence in situ hybridization and spectral karyotyping reveals hidden genetic aberrations in children with acute lymphoblastic leukaemia and a normal banded karyotypeA Nordgren, J Schoumans, S Söderhäll, et al.
Clinical Genetics|May 22, 2010
High-resolution molecular karyotyping in patients with developmental delay and/or multiple congenital anomalies in a clinical settingJ Wincent, B-M Anderlid, M Lagerberg, et al.
Journal of Medical Genetics|February 27, 2004
The performance of CGH array for the detection of cryptic constitutional chromosome imbalancesJ Schoumans, B-M Anderlid, E Blennow, et al.
Clinical Genetics|May 1, 2008
Concurrent microdeletion and duplication of 22q11.2E Blennow, K Lagerstedt, H Malmgren, et al.
Clinical Genetics|March 19, 2010
Improved structural characterization of chromosomal breakpoints using high resolution custom array-CGHA Lindstrand, J Schoumans, P Gustavsson, et al.
American Journal of Medical Genetics. Part A|November 14, 2008
Molecular cytogenetic characterization of a constitutional, highly complex intrachromosomal rearrangement of chromosome 1, with 14 breakpoints and a 0.5 Mb submicroscopic deletionA Lindstrand, H Malmgren, S Sahlén, et al.
Journal of Medical Genetics|September 6, 2005
Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH)J Schoumans, C Ruivenkamp, E Holmberg, et al.
Leukemia|October 1, 2004
Raji revisited: cytogenetics of the original Burkitt's lymphoma cell lineM B Karpova, J Schoumans, I Ernberg, et al.
American Journal of Medical Genetics|March 10, 2001
Detailed characterization of 12 supernumerary ring chromosomes using micro-FISH and search for uniparental disomyB M Anderlid, S Sahlén, J Schoumans, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Cytogenetic and Genome Research|November 17, 2011
Interpretation of array comparative genome hybridization data: a major challengeA C J Gijsbers, J Schoumans, C A L Ruivenkamp
British Journal of Haematology|September 21, 2001
Interphase fluorescence in situ hybridization and spectral karyotyping reveals hidden genetic aberrations in children with acute lymphoblastic leukaemia and a normal banded karyotypeA Nordgren, J Schoumans, S Söderhäll, et al.
Clinical Genetics|May 22, 2010
High-resolution molecular karyotyping in patients with developmental delay and/or multiple congenital anomalies in a clinical settingJ Wincent, B-M Anderlid, M Lagerberg, et al.
Journal of Medical Genetics|February 27, 2004
The performance of CGH array for the detection of cryptic constitutional chromosome imbalancesJ Schoumans, B-M Anderlid, E Blennow, et al.
Clinical Genetics|May 1, 2008
Concurrent microdeletion and duplication of 22q11.2E Blennow, K Lagerstedt, H Malmgren, et al.
Clinical Genetics|March 19, 2010
Improved structural characterization of chromosomal breakpoints using high resolution custom array-CGHA Lindstrand, J Schoumans, P Gustavsson, et al.
American Journal of Medical Genetics. Part A|November 14, 2008
Molecular cytogenetic characterization of a constitutional, highly complex intrachromosomal rearrangement of chromosome 1, with 14 breakpoints and a 0.5 Mb submicroscopic deletionA Lindstrand, H Malmgren, S Sahlén, et al.
Journal of Medical Genetics|September 6, 2005
Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH)J Schoumans, C Ruivenkamp, E Holmberg, et al.
Leukemia|October 1, 2004
Raji revisited: cytogenetics of the original Burkitt's lymphoma cell lineM B Karpova, J Schoumans, I Ernberg, et al.
American Journal of Medical Genetics|March 10, 2001
Detailed characterization of 12 supernumerary ring chromosomes using micro-FISH and search for uniparental disomyB M Anderlid, S Sahlén, J Schoumans, et al.
Pageof 3