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

de la CHAPELLE

Showing results (101-110 of 603) with videos related to

Pageof 61
Sort By:
Neuromuscular Disorders : NMD|May 1, 1995
Muscle-eye-brain disease and Fukuyama type congenital muscular dystrophy are not allelicS Ranta, H Pihko, P Santavuori, et al.
Journal of Medical Genetics|April 1, 1993
Prenatal diagnosis of diastrophic dysplasia with polymorphic DNA markersJ Hästbacka, R Salonen, P Laurila, et al.
Clinical Genetics|June 1, 1987
Pallister-Killian syndrome: cytogenetic and molecular studiesP Peltomäki, S Knuutila, A Ritvanen, et al.
Journal of Microscopy|March 12, 2008
Modelling of the near-field of metallic nanoparticle gratings: localized surface plasmon resonance and SERS applicationsA-S Grimault, A Vial, J Grand, et al.
Cancer Genetics and Cytogenetics|February 1, 1985
t(11;19)(q23;p11) in a child with acute T-cell leukemiaS Knuutila, J Rajantie, R Leskinen, et al.
American Journal of Human Genetics|May 1, 1997
Linkage disequilibrium and physical mapping of X-linked juvenile retinoschisisL Huopaniemi, A Rantala, E Tahvanainen, et al.
Lancet (London, England)|January 9, 1993
Familial erythrocytosis genetically linked to erythropoietin receptor geneA de la Chapelle, P Sistonen, H Lehväslaiho, et al.
Human Genetics|January 1, 1983
Protein A radio-assay of H-Y antigen on human leukocytes using mouse and rat antisera and monoclonal antibodiesH Savikurki, L C Andersson, S S Wachtel, et al.
Cancer Genetics and Cytogenetics|April 1, 1984
Critical chromosome rearrangement in acute promyelocytic leukemiaS Knuutila, T Ruutu, R Kovanen, et al.
Biochimica Et Biophysica Acta|April 12, 1989
The methylation pattern of normal and truncated amplified human c-myc oncogenesN O Bianchi, M S Bianchi, K Alitalo, et al.
Pageof 61

Showing results (101-110 of 603) with videos related to

Sort By:
Pageof 61
Neuromuscular Disorders : NMD|May 1, 1995
Muscle-eye-brain disease and Fukuyama type congenital muscular dystrophy are not allelicS Ranta, H Pihko, P Santavuori, et al.
Journal of Medical Genetics|April 1, 1993
Prenatal diagnosis of diastrophic dysplasia with polymorphic DNA markersJ Hästbacka, R Salonen, P Laurila, et al.
Clinical Genetics|June 1, 1987
Pallister-Killian syndrome: cytogenetic and molecular studiesP Peltomäki, S Knuutila, A Ritvanen, et al.
Journal of Microscopy|March 12, 2008
Modelling of the near-field of metallic nanoparticle gratings: localized surface plasmon resonance and SERS applicationsA-S Grimault, A Vial, J Grand, et al.
Cancer Genetics and Cytogenetics|February 1, 1985
t(11;19)(q23;p11) in a child with acute T-cell leukemiaS Knuutila, J Rajantie, R Leskinen, et al.
American Journal of Human Genetics|May 1, 1997
Linkage disequilibrium and physical mapping of X-linked juvenile retinoschisisL Huopaniemi, A Rantala, E Tahvanainen, et al.
Lancet (London, England)|January 9, 1993
Familial erythrocytosis genetically linked to erythropoietin receptor geneA de la Chapelle, P Sistonen, H Lehväslaiho, et al.
Human Genetics|January 1, 1983
Protein A radio-assay of H-Y antigen on human leukocytes using mouse and rat antisera and monoclonal antibodiesH Savikurki, L C Andersson, S S Wachtel, et al.
Cancer Genetics and Cytogenetics|April 1, 1984
Critical chromosome rearrangement in acute promyelocytic leukemiaS Knuutila, T Ruutu, R Kovanen, et al.
Biochimica Et Biophysica Acta|April 12, 1989
The methylation pattern of normal and truncated amplified human c-myc oncogenesN O Bianchi, M S Bianchi, K Alitalo, et al.
Pageof 61