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

C Verellen

Showing results (11-20 of 77) with videos related to

Pageof 8
Sort By:
Advances in Nephrology From the Necker Hospital|November 9, 2000
Autosomal-dominant chronic interstitial nephritis with early hyperuricemiaY Pirson, G Loute, J P Cosyns, et al.
Acta Clinica Belgica|December 7, 2010
Chorea associated with anti-phospholipid antibodies: case reportJ Demonty, M Gonce, P Ribai, et al.
Acta Neurologica Belgica|January 25, 2020
Hereditary axonal neuropathy related to MME gene mutation in a family with fetomaternal alloimmune glomerulonephritisM Dupuis, J M Raymackers, N Ackermans, et al.
Journal of Medical Genetics|November 1, 1994
High CTG repeat number in nodular thyroid tissue from a myotonic dystrophy patientC Daumerie, N Lannoy, J P Squifflet, et al.
American Journal of Medical Genetics|May 15, 1993
Oral-facial-digital syndrome type I in a newborn maleY Gillerot, M Heimann, C Fourneau, et al.
Journal of Medical Genetics|November 10, 2000
A CGC>CAT gene conversion-like event resulting in the R122H mutation in the cationic trypsinogen gene and its implication in the genotyping of pancreatitisJ M Chen, O Raguenes, C Ferec, et al.
Archives Francaises De Pediatrie|December 1, 1989
[Deletion of the long arm of chromosome 18, primary hypothyroidism, Biermer's anemia and IgM hypogammaglobulinemia]B Henrot, J Ninane, C Mercenier, et al.
Journal De Genetique Humaine|November 1, 1976
[Association of ocular and otological damage in an institution for the visually and mentally handicapped]J F Cuendet, E Juillard, A Catti, et al.
The Journal of Pediatrics|November 5, 1997
Very long chain acyl-coenzyme A dehydrogenase deficiency in two siblings: evolution after prenatal diagnosis and prompt managementT Sluysmans, D Tuerlinckx, C Hubinont, et al.
Prenatal Diagnosis|July 1, 1984
S-100 protein in amniotic fluid of anencephalic fetusesC J Sindic, M Freund, N Van Regemorter, et al.
Pageof 8

Showing results (11-20 of 77) with videos related to

Sort By:
Pageof 8
Advances in Nephrology From the Necker Hospital|November 9, 2000
Autosomal-dominant chronic interstitial nephritis with early hyperuricemiaY Pirson, G Loute, J P Cosyns, et al.
Acta Clinica Belgica|December 7, 2010
Chorea associated with anti-phospholipid antibodies: case reportJ Demonty, M Gonce, P Ribai, et al.
Acta Neurologica Belgica|January 25, 2020
Hereditary axonal neuropathy related to MME gene mutation in a family with fetomaternal alloimmune glomerulonephritisM Dupuis, J M Raymackers, N Ackermans, et al.
Journal of Medical Genetics|November 1, 1994
High CTG repeat number in nodular thyroid tissue from a myotonic dystrophy patientC Daumerie, N Lannoy, J P Squifflet, et al.
American Journal of Medical Genetics|May 15, 1993
Oral-facial-digital syndrome type I in a newborn maleY Gillerot, M Heimann, C Fourneau, et al.
Journal of Medical Genetics|November 10, 2000
A CGC>CAT gene conversion-like event resulting in the R122H mutation in the cationic trypsinogen gene and its implication in the genotyping of pancreatitisJ M Chen, O Raguenes, C Ferec, et al.
Archives Francaises De Pediatrie|December 1, 1989
[Deletion of the long arm of chromosome 18, primary hypothyroidism, Biermer's anemia and IgM hypogammaglobulinemia]B Henrot, J Ninane, C Mercenier, et al.
Journal De Genetique Humaine|November 1, 1976
[Association of ocular and otological damage in an institution for the visually and mentally handicapped]J F Cuendet, E Juillard, A Catti, et al.
The Journal of Pediatrics|November 5, 1997
Very long chain acyl-coenzyme A dehydrogenase deficiency in two siblings: evolution after prenatal diagnosis and prompt managementT Sluysmans, D Tuerlinckx, C Hubinont, et al.
Prenatal Diagnosis|July 1, 1984
S-100 protein in amniotic fluid of anencephalic fetusesC J Sindic, M Freund, N Van Regemorter, et al.
Pageof 8