Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J Schoumans

Showing results (11-20 of 23) with videos related to

Pageof 3
Sort By:
Clinical Genetics|May 3, 2006
Hemizygosity for chromosome 2q14.2-q22.1 spanning the GLI2 and PROC genes associated with growth hormone deficiency, polydactyly, deep vein thrombosis and urogenital abnormalitiesP Gustavsson, J Schoumans, J Staaf, et al.
Clinical Genetics|May 1, 2008
CHD7 mutation spectrum in 28 Swedish patients diagnosed with CHARGE syndromeJ Wincent, E Holmberg, K Strömland, et al.
Leukemia|June 22, 2013
Detecting dic(9;20)(p13.2;p11.2)-positive B-cell precursor acute lymphoblastic leukemia in a clinical setting using fluorescence in situ hybridizationV Zachariadis, J Schoumans, I Ofverholm, et al.
Clinical Genetics|October 30, 2009
Detailed molecular and clinical characterization of three patients with 21q deletionsA Lindstrand, H Malmgren, S Sahlén, et al.
Leukemia|February 23, 2007
Tiling-resolution array-CGH reveals the pattern of DNA copy number alterations in acute lymphoblastic leukemia with 21q amplification: the result of telomere dysfunction and breakage/fusion/breakage cycles?E Kuchinskaya, A Nordgren, M Heyman, et al.
Journal of Medical Genetics|September 18, 2007
Genotype-phenotype correlation in 21 patients with Wolf-Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH)N M C Maas, G Van Buggenhout, F Hannes, et al.
Leukemia|January 19, 2011
The frequency and prognostic impact of dic(9;20)(p13.2;q11.2) in childhood B-cell precursor acute lymphoblastic leukemia: results from the NOPHO ALL-2000 trialV Zachariadis, F Gauffin, E Kuchinskaya, et al.
Leukemia|February 12, 2020
European recommendations and quality assurance for cytogenomic analysis of haematological neoplasms: reponse to the comments from the Francophone Group of Hematological Cytogenetics (GFCH)K A Rack, E van den Berg, C Haferlach, et al.
Leukemia|January 31, 2019
European recommendations and quality assurance for cytogenomic analysis of haematological neoplasmsK A Rack, E van den Berg, C Haferlach, et al.
Human Genetics|December 6, 2001
Analysis of short stature homeobox-containing gene ( SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformityG Grigelioniene, J Schoumans, L Neumeyer, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Clinical Genetics|May 3, 2006
Hemizygosity for chromosome 2q14.2-q22.1 spanning the GLI2 and PROC genes associated with growth hormone deficiency, polydactyly, deep vein thrombosis and urogenital abnormalitiesP Gustavsson, J Schoumans, J Staaf, et al.
Clinical Genetics|May 1, 2008
CHD7 mutation spectrum in 28 Swedish patients diagnosed with CHARGE syndromeJ Wincent, E Holmberg, K Strömland, et al.
Leukemia|June 22, 2013
Detecting dic(9;20)(p13.2;p11.2)-positive B-cell precursor acute lymphoblastic leukemia in a clinical setting using fluorescence in situ hybridizationV Zachariadis, J Schoumans, I Ofverholm, et al.
Clinical Genetics|October 30, 2009
Detailed molecular and clinical characterization of three patients with 21q deletionsA Lindstrand, H Malmgren, S Sahlén, et al.
Leukemia|February 23, 2007
Tiling-resolution array-CGH reveals the pattern of DNA copy number alterations in acute lymphoblastic leukemia with 21q amplification: the result of telomere dysfunction and breakage/fusion/breakage cycles?E Kuchinskaya, A Nordgren, M Heyman, et al.
Journal of Medical Genetics|September 18, 2007
Genotype-phenotype correlation in 21 patients with Wolf-Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH)N M C Maas, G Van Buggenhout, F Hannes, et al.
Leukemia|January 19, 2011
The frequency and prognostic impact of dic(9;20)(p13.2;q11.2) in childhood B-cell precursor acute lymphoblastic leukemia: results from the NOPHO ALL-2000 trialV Zachariadis, F Gauffin, E Kuchinskaya, et al.
Leukemia|February 12, 2020
European recommendations and quality assurance for cytogenomic analysis of haematological neoplasms: reponse to the comments from the Francophone Group of Hematological Cytogenetics (GFCH)K A Rack, E van den Berg, C Haferlach, et al.
Leukemia|January 31, 2019
European recommendations and quality assurance for cytogenomic analysis of haematological neoplasmsK A Rack, E van den Berg, C Haferlach, et al.
Human Genetics|December 6, 2001
Analysis of short stature homeobox-containing gene ( SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformityG Grigelioniene, J Schoumans, L Neumeyer, et al.
Pageof 3