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H Puissant

Showing results (1-10 of 9) with videos related to

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La Revue Du Praticien|October 29, 1987
[Detection of karyotype abnormalities]L Larget-Piet, A Larget-Piet, H Puissant
Human Genetics|July 1, 1988
Molecular analysis of a reciprocal translocation t(5;11) (q11;p13) in a WAGR patientH Puissant, M Azoulay, J L Serre, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1983
Reactivating factors of human alpha-mannosidase mutantM C Miranda, S Gautron, H Puissant, et al.
Human Genetics|January 1, 1983
Evidence for the presence of beta-subunit of hexosaminidase in a case of Sandhoff disease using a blotting techniqueS Gautron, L Poenaru, J Boue, et al.
Archives Francaises De Pediatrie|August 1, 1990
[Direct diagnosis of predominant mutation delta F508 associated with the mucoviscidosis gene]C Férec, H Guillermit, C Verlingue, et al.
American Journal of Medical Genetics|March 1, 1989
Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomaliesC Turleau, M O Cabanis, D Girault, 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.
Journal De Genetique Humaine|January 1, 1987
[What course should be adopted after the discovery of a gonosome anomaly in the fetal karyotype?]B Le Marec, L Larget-Piet, A Larget-Piet, et al.
American Journal of Medical Genetics|December 1, 1994
Molecular analysis of 53 fragile X families with the probe StB12.3H Puissant, M C Malinge, A Larget-Piet, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
La Revue Du Praticien|October 29, 1987
[Detection of karyotype abnormalities]L Larget-Piet, A Larget-Piet, H Puissant
Human Genetics|July 1, 1988
Molecular analysis of a reciprocal translocation t(5;11) (q11;p13) in a WAGR patientH Puissant, M Azoulay, J L Serre, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1983
Reactivating factors of human alpha-mannosidase mutantM C Miranda, S Gautron, H Puissant, et al.
Human Genetics|January 1, 1983
Evidence for the presence of beta-subunit of hexosaminidase in a case of Sandhoff disease using a blotting techniqueS Gautron, L Poenaru, J Boue, et al.
Archives Francaises De Pediatrie|August 1, 1990
[Direct diagnosis of predominant mutation delta F508 associated with the mucoviscidosis gene]C Férec, H Guillermit, C Verlingue, et al.
American Journal of Medical Genetics|March 1, 1989
Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomaliesC Turleau, M O Cabanis, D Girault, 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.
Journal De Genetique Humaine|January 1, 1987
[What course should be adopted after the discovery of a gonosome anomaly in the fetal karyotype?]B Le Marec, L Larget-Piet, A Larget-Piet, et al.
American Journal of Medical Genetics|December 1, 1994
Molecular analysis of 53 fragile X families with the probe StB12.3H Puissant, M C Malinge, A Larget-Piet, et al.
Pageof 1