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

P Malet

Showing results (51-60 of 86) with videos related to

Pageof 9
Sort By:
Cancer Genetics and Cytogenetics|February 1, 1986
Translocation t(3;20) associated with thrombocythemia in Ph-positive CMLM F Turchini, P Travade, A De Larocque, et al.
Cancer Genetics and Cytogenetics|October 1, 1983
Chronic myelogenous leukemia (CML) with translocation (8;22): a new variantM F Turchini, A Geneix, A Delaroque, et al.
Analytical Cellular Pathology : the Journal of the European Society for Analytical Cellular Pathology|October 1, 1994
Rapid identification of marker chromosomes by in situ hybridization under different stringency conditionsS G Vorsanova, Y B Yurov, I V Soloviev, et al.
Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences. Serie D: Sciences Naturelles|November 14, 1977
[Immunocytochemical labeling of human chromosomes by antibodies from human autoimmune serum]J Morin, M Marcollet, A Geneix, et al.
Cancer Genetics and Cytogenetics|April 15, 1985
Insertion of part of chromosome 5 into chromosome 1 in a case of sideroblastic anemia with an excess of blastsM F Turchini, P Travade, A Geneix, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1992
[Complete and homogenous trisomy 9 detected in utero]F Raffi, A Geneix, D Satge, et al.
Prenatal Diagnosis|March 1, 1995
Prenatal diagnosis of trisomy 21 using interphase fluorescence in situ hybridization of post-replicated cells with site-specific cosmid and cosmid contig probesI V Soloviev, Y B Yurov, S G Vorsanova, et al.
Clinical Genetics|December 1, 1996
A history of miscarriages and mild prognathism as possible mode of presentation of mosaic trisomy 18 in womenD Satge, A Geneix, J Goburdhun, et al.
Pathologie-Biologie|February 1, 1986
[Contribution of electron microscopy of cultures of fibroblasts in the diagnosis of hereditary metabolic diseases]J Y Jaffray, F Charbonne, P Rousseau, et al.
Cancer Genetics and Cytogenetics|June 1, 1984
Cytogenetic studies in a case of T-cell prolymphocytic leukemiaM F Turchini, A Geneix, P Travade, et al.
Pageof 9

Showing results (51-60 of 86) with videos related to

Sort By:
Pageof 9
Cancer Genetics and Cytogenetics|February 1, 1986
Translocation t(3;20) associated with thrombocythemia in Ph-positive CMLM F Turchini, P Travade, A De Larocque, et al.
Cancer Genetics and Cytogenetics|October 1, 1983
Chronic myelogenous leukemia (CML) with translocation (8;22): a new variantM F Turchini, A Geneix, A Delaroque, et al.
Analytical Cellular Pathology : the Journal of the European Society for Analytical Cellular Pathology|October 1, 1994
Rapid identification of marker chromosomes by in situ hybridization under different stringency conditionsS G Vorsanova, Y B Yurov, I V Soloviev, et al.
Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences. Serie D: Sciences Naturelles|November 14, 1977
[Immunocytochemical labeling of human chromosomes by antibodies from human autoimmune serum]J Morin, M Marcollet, A Geneix, et al.
Cancer Genetics and Cytogenetics|April 15, 1985
Insertion of part of chromosome 5 into chromosome 1 in a case of sideroblastic anemia with an excess of blastsM F Turchini, P Travade, A Geneix, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1992
[Complete and homogenous trisomy 9 detected in utero]F Raffi, A Geneix, D Satge, et al.
Prenatal Diagnosis|March 1, 1995
Prenatal diagnosis of trisomy 21 using interphase fluorescence in situ hybridization of post-replicated cells with site-specific cosmid and cosmid contig probesI V Soloviev, Y B Yurov, S G Vorsanova, et al.
Clinical Genetics|December 1, 1996
A history of miscarriages and mild prognathism as possible mode of presentation of mosaic trisomy 18 in womenD Satge, A Geneix, J Goburdhun, et al.
Pathologie-Biologie|February 1, 1986
[Contribution of electron microscopy of cultures of fibroblasts in the diagnosis of hereditary metabolic diseases]J Y Jaffray, F Charbonne, P Rousseau, et al.
Cancer Genetics and Cytogenetics|June 1, 1984
Cytogenetic studies in a case of T-cell prolymphocytic leukemiaM F Turchini, A Geneix, P Travade, et al.
Pageof 9