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 Gubler

Showing results (181-190 of 195) with videos related to

Pageof 20
Sort By:
Human Genetics|December 1, 1992
Alport syndrome: a genetic study of 31 familiesR M'Rad, M Sanak, G Deschenes, et al.
Prenatal Diagnosis|April 2, 2004
Sonographic findings in Beckwith-Wiedemann syndrome related to H19 hypermethylationC Le Caignec, C Gicquel, M C Gubler, et al.
Saudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|September 15, 2006
Autosomal dominant Alport's syndrome: study of a large Tunisian familyM Kharrat, S Makni, K Makni, et al.
American Journal of Human Genetics|October 30, 1998
Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndromeE Boye, G Mollet, L Forestier, et al.
Kidney International|May 3, 2000
WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosisE Denamur, N Bocquet, V Baudouin, et al.
Journal of Medical Genetics|April 5, 2005
Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohortsA M Sharp, L M Messiaen, G Page, et al.
Pediatric Nephrology (Berlin, Germany)|January 23, 1998
Chronic renal failure and cranioectodermal dysplasia: a further stepM Tsimaratos, E Bérard, S Sigaudy, et al.
Nature Genetics|September 1, 1994
Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndromeT Mochizuki, H H Lemmink, M Mariyama, et al.
Kidney International. Supplement|May 1, 1982
Alport's syndrome: experience at Hôpital NeckerR Habib, M C Gubler, N Hinglais, et al.
American Journal of Human Genetics|December 1, 1996
Spectrum of mutations in the COL4A5 collagen gene in X-linked Alport syndromeB Knebelmann, C Breillat, L Forestier, et al.
Pageof 20

Showing results (181-190 of 195) with videos related to

Sort By:
Pageof 20
Human Genetics|December 1, 1992
Alport syndrome: a genetic study of 31 familiesR M'Rad, M Sanak, G Deschenes, et al.
Prenatal Diagnosis|April 2, 2004
Sonographic findings in Beckwith-Wiedemann syndrome related to H19 hypermethylationC Le Caignec, C Gicquel, M C Gubler, et al.
Saudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|September 15, 2006
Autosomal dominant Alport's syndrome: study of a large Tunisian familyM Kharrat, S Makni, K Makni, et al.
American Journal of Human Genetics|October 30, 1998
Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndromeE Boye, G Mollet, L Forestier, et al.
Kidney International|May 3, 2000
WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosisE Denamur, N Bocquet, V Baudouin, et al.
Journal of Medical Genetics|April 5, 2005
Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohortsA M Sharp, L M Messiaen, G Page, et al.
Pediatric Nephrology (Berlin, Germany)|January 23, 1998
Chronic renal failure and cranioectodermal dysplasia: a further stepM Tsimaratos, E Bérard, S Sigaudy, et al.
Nature Genetics|September 1, 1994
Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndromeT Mochizuki, H H Lemmink, M Mariyama, et al.
Kidney International. Supplement|May 1, 1982
Alport's syndrome: experience at Hôpital NeckerR Habib, M C Gubler, N Hinglais, et al.
American Journal of Human Genetics|December 1, 1996
Spectrum of mutations in the COL4A5 collagen gene in X-linked Alport syndromeB Knebelmann, C Breillat, L Forestier, et al.
Pageof 20