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V Cacheux

Showing results (21-30 of 28) with videos related to

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Blood|April 1, 1996
The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemiaS Raynaud, H Cave, M Baens, et al.
Annales De Genetique|December 2, 1998
Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalitiesJ M Lapierre, V Cacheux, N Collot, et al.
Bone Marrow Transplantation|November 3, 2010
Retrospective study of allogeneic haematopoietic stem-cell transplantation for myelofibrosisS Lissandre, J-O Bay, J-Y Cahn, et al.
Nature Genetics|June 3, 2000
Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiencyI Netchine, M L Sobrier, H Krude, et al.
FEBS Letters|November 21, 1998
Human Prop-1: cloning, mapping, genomic structure. Mutations in familial combined pituitary hormone deficiencyP Duquesnoy, A Roy, F Dastot, et al.
Annales De Genetique|January 1, 1997
Systematic screening for fragile X syndrome in a cohort of 574 mentally retarded childrenB Gérard, M F Le Heuzey, G Brunie, et al.
Blood|March 1, 1996
Expression of p13MTCP1 is restricted to mature T-cell proliferations with t(X;14) translocationsA Madani, V Choukroun, J Soulier, et al.
Journal of Medical Genetics|November 19, 2008
Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practiceD L Bruno, D Ganesamoorthy, J Schoumans, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Blood|April 1, 1996
The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemiaS Raynaud, H Cave, M Baens, et al.
Annales De Genetique|December 2, 1998
Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalitiesJ M Lapierre, V Cacheux, N Collot, et al.
Bone Marrow Transplantation|November 3, 2010
Retrospective study of allogeneic haematopoietic stem-cell transplantation for myelofibrosisS Lissandre, J-O Bay, J-Y Cahn, et al.
Nature Genetics|June 3, 2000
Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiencyI Netchine, M L Sobrier, H Krude, et al.
FEBS Letters|November 21, 1998
Human Prop-1: cloning, mapping, genomic structure. Mutations in familial combined pituitary hormone deficiencyP Duquesnoy, A Roy, F Dastot, et al.
Annales De Genetique|January 1, 1997
Systematic screening for fragile X syndrome in a cohort of 574 mentally retarded childrenB Gérard, M F Le Heuzey, G Brunie, et al.
Blood|March 1, 1996
Expression of p13MTCP1 is restricted to mature T-cell proliferations with t(X;14) translocationsA Madani, V Choukroun, J Soulier, et al.
Journal of Medical Genetics|November 19, 2008
Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practiceD L Bruno, D Ganesamoorthy, J Schoumans, et al.
Pageof 3