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 L Mandel

Showing results (191-200 of 257) with videos related to

Pageof 26
Sort By:
The New England Journal of Medicine|October 17, 1996
Clinical and genetic abnormalities in patients with Friedreich's ataxiaA Dürr, M Cossee, Y Agid, et al.
Lancet (London, England)|October 20, 1984
Exclusion of haemophilia B in male fetus by chorionic villus biopsyT Tønnesen, F Søndergaard, F Güttler, et al.
The New England Journal of Medicine|March 14, 1985
Genetic screening for hemophilia A (classic hemophilia) with a polymorphic DNA probeI Oberle, G Camerino, R Heilig, et al.
American Journal of Medical Genetics|May 1, 1988
Linkage analysis suggests at least two loci for X-linked non-specific mental retardationB Arveiler, Y Alembik, A Hanauer, et al.
Science (New York, N.Y.)|May 24, 1991
Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndromeI Oberlé, F Rousseau, D Heitz, et al.
American Journal of Medical Genetics|April 1, 1992
Fifth international workshop on fragile X and X-linked mental retardationJ L Mandel, R Hagerman, U Froster, et al.
American Journal of Medical Genetics|May 1, 1988
Probable localisation of the Coffin-Lowry locus in Xp22.2-p22.1 by multipoint linkage analysisA Hanauer, Y Alembik, S Gilgenkrantz, et al.
Human Genetics|January 1, 1985
First trimester prenatal diagnosis of adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis to a DNA probeJ Boué, I Oberle, R Heilig, et al.
Lancet (London, England)|May 6, 1995
Rapid antibody test for fragile X syndromeR Willemsen, S Mohkamsing, B de Vries, et al.
Nature|December 12, 1996
Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndromeE Trivier, D De Cesare, S Jacquot, et al.
Pageof 26

Showing results (191-200 of 257) with videos related to

Sort By:
Pageof 26
The New England Journal of Medicine|October 17, 1996
Clinical and genetic abnormalities in patients with Friedreich's ataxiaA Dürr, M Cossee, Y Agid, et al.
Lancet (London, England)|October 20, 1984
Exclusion of haemophilia B in male fetus by chorionic villus biopsyT Tønnesen, F Søndergaard, F Güttler, et al.
The New England Journal of Medicine|March 14, 1985
Genetic screening for hemophilia A (classic hemophilia) with a polymorphic DNA probeI Oberle, G Camerino, R Heilig, et al.
American Journal of Medical Genetics|May 1, 1988
Linkage analysis suggests at least two loci for X-linked non-specific mental retardationB Arveiler, Y Alembik, A Hanauer, et al.
Science (New York, N.Y.)|May 24, 1991
Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndromeI Oberlé, F Rousseau, D Heitz, et al.
American Journal of Medical Genetics|April 1, 1992
Fifth international workshop on fragile X and X-linked mental retardationJ L Mandel, R Hagerman, U Froster, et al.
American Journal of Medical Genetics|May 1, 1988
Probable localisation of the Coffin-Lowry locus in Xp22.2-p22.1 by multipoint linkage analysisA Hanauer, Y Alembik, S Gilgenkrantz, et al.
Human Genetics|January 1, 1985
First trimester prenatal diagnosis of adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis to a DNA probeJ Boué, I Oberle, R Heilig, et al.
Lancet (London, England)|May 6, 1995
Rapid antibody test for fragile X syndromeR Willemsen, S Mohkamsing, B de Vries, et al.
Nature|December 12, 1996
Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndromeE Trivier, D De Cesare, S Jacquot, et al.
Pageof 26