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 (141-150 of 603) with videos related to

Pageof 61
Sort By:
Cell|June 5, 1987
An abnormal terminal X-Y interchange accounts for most but not all cases of human XX malenessC Petit, A de la Chapelle, J Levilliers, et al.
Leukemia|June 1, 1989
Human bone marrow cytogenetics: growth factors stimulate metaphases for specific lineagesM Keinänen, C D Bloomfield, J Machnicki, et al.
Cancer Genetics and Cytogenetics|March 1, 1987
Constitutional translocation t(3;6)(p14;p11) in a family with hematologic malignanciesA Markkanen, T Ruutu, V Rasi, et al.
Genomics|March 8, 2000
A sequence-ready map of the Usher syndrome type III critical region on chromosome 3qT Joensuu, R Hämäläinen, A E Lehesjoki, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Three widespread founder mutations contribute to high incidence of X-linked juvenile retinoschisis in FinlandL Huopaniemi, A Rantala, H Forsius, et al.
American Journal of Human Genetics|January 1, 1991
Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysisT Alitalo, T A Kruse, H Forsius, et al.
Neurology|November 1, 1993
Progressive myoclonus epilepsy of Unverricht-Lundborg type: a clinical and molecular genetic study of a family from the United States with four affected sibsA E Lehesjoki, R Eldridge, J Eldridge, et al.
Scandinavian Journal of Haematology|December 1, 1975
Transplacental passage of foetal blood cellsR Zilliacus, A De la Chapelle, J Schröder, et al.
Blood|December 1, 1985
t(1;3)(p36;q21) in acute nonlymphocytic leukemia: a new cytogenetic-clinicopathologic associationC D Bloomfield, O M Garson, L Volin, et al.
British Journal of Haematology|October 27, 2007
Molecular profiling of chronic lymphocytic leukaemia: genetics meets epigenetics to identify predisposing genesChristoph Plass, John C Byrd, Aparna Raval, et al.
Pageof 61

Showing results (141-150 of 603) with videos related to

Sort By:
Pageof 61
Cell|June 5, 1987
An abnormal terminal X-Y interchange accounts for most but not all cases of human XX malenessC Petit, A de la Chapelle, J Levilliers, et al.
Leukemia|June 1, 1989
Human bone marrow cytogenetics: growth factors stimulate metaphases for specific lineagesM Keinänen, C D Bloomfield, J Machnicki, et al.
Cancer Genetics and Cytogenetics|March 1, 1987
Constitutional translocation t(3;6)(p14;p11) in a family with hematologic malignanciesA Markkanen, T Ruutu, V Rasi, et al.
Genomics|March 8, 2000
A sequence-ready map of the Usher syndrome type III critical region on chromosome 3qT Joensuu, R Hämäläinen, A E Lehesjoki, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Three widespread founder mutations contribute to high incidence of X-linked juvenile retinoschisis in FinlandL Huopaniemi, A Rantala, H Forsius, et al.
American Journal of Human Genetics|January 1, 1991
Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysisT Alitalo, T A Kruse, H Forsius, et al.
Neurology|November 1, 1993
Progressive myoclonus epilepsy of Unverricht-Lundborg type: a clinical and molecular genetic study of a family from the United States with four affected sibsA E Lehesjoki, R Eldridge, J Eldridge, et al.
Scandinavian Journal of Haematology|December 1, 1975
Transplacental passage of foetal blood cellsR Zilliacus, A De la Chapelle, J Schröder, et al.
Blood|December 1, 1985
t(1;3)(p36;q21) in acute nonlymphocytic leukemia: a new cytogenetic-clinicopathologic associationC D Bloomfield, O M Garson, L Volin, et al.
British Journal of Haematology|October 27, 2007
Molecular profiling of chronic lymphocytic leukaemia: genetics meets epigenetics to identify predisposing genesChristoph Plass, John C Byrd, Aparna Raval, et al.
Pageof 61