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

D Bonneau

Showing results (111-120 of 143) with videos related to

Pageof 15
Sort By:
Journal of Medical Genetics|December 1, 1998
Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotypeM Longy, V Coulon, B Duboué, et al.
Surgery|December 22, 1999
Mapping of a gene predisposing to familial thyroid tumors with cell oxyphilia to chromosome 19 and exclusion of JUN B as a candidate geneJ L Kraimps, F Canzian, C Jost, et al.
Genomics|May 1, 1994
Genetic heterogeneity of Usher syndrome type 1 in French familiesD Larget-Piet, S Gerber, D Bonneau, et al.
JIMD Reports|November 14, 2015
In Utero Diagnosis of Niemann-Pick Type C in the Absence of Family HistoryE Colin, M Barth, F Boussion, et al.
European Journal of Medical Genetics|October 8, 2009
Oculo-dento-digital dysplasia: lack of genotype-phenotype correlation for GJA1 mutations and usefulness of neuro-imagingM J Alao, D Bonneau, M Holder-Espinasse, et al.
Neurology|February 22, 2008
Multiple sclerosis-like disorder in OPA1-related autosomal dominant optic atrophyC Verny, D Loiseau, C Scherer, et al.
Prenatal Diagnosis|October 18, 2008
Influence of ultrasonographers training on prenatal diagnosis of congenital heart diseases: a 12-year population-based studyPh Pézard, L Bonnemains, F Boussion, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|November 16, 2011
Binder phenotype in mothers affected with autoimmune disordersE Colin, R Touraine, J M Levaillant, et al.
Eye (London, England)|November 19, 2016
Multiethnic involvement in autosomal-dominant optic atrophy in SingaporeJ L Loo, S Singhal, A V Rukmini, et al.
Neurology|April 27, 2011
Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMTJ Cassereau, C Casasnovas, N Gueguen, et al.
Pageof 15

Showing results (111-120 of 143) with videos related to

Sort By:
Pageof 15
Journal of Medical Genetics|December 1, 1998
Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotypeM Longy, V Coulon, B Duboué, et al.
Surgery|December 22, 1999
Mapping of a gene predisposing to familial thyroid tumors with cell oxyphilia to chromosome 19 and exclusion of JUN B as a candidate geneJ L Kraimps, F Canzian, C Jost, et al.
Genomics|May 1, 1994
Genetic heterogeneity of Usher syndrome type 1 in French familiesD Larget-Piet, S Gerber, D Bonneau, et al.
JIMD Reports|November 14, 2015
In Utero Diagnosis of Niemann-Pick Type C in the Absence of Family HistoryE Colin, M Barth, F Boussion, et al.
European Journal of Medical Genetics|October 8, 2009
Oculo-dento-digital dysplasia: lack of genotype-phenotype correlation for GJA1 mutations and usefulness of neuro-imagingM J Alao, D Bonneau, M Holder-Espinasse, et al.
Neurology|February 22, 2008
Multiple sclerosis-like disorder in OPA1-related autosomal dominant optic atrophyC Verny, D Loiseau, C Scherer, et al.
Prenatal Diagnosis|October 18, 2008
Influence of ultrasonographers training on prenatal diagnosis of congenital heart diseases: a 12-year population-based studyPh Pézard, L Bonnemains, F Boussion, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|November 16, 2011
Binder phenotype in mothers affected with autoimmune disordersE Colin, R Touraine, J M Levaillant, et al.
Eye (London, England)|November 19, 2016
Multiethnic involvement in autosomal-dominant optic atrophy in SingaporeJ L Loo, S Singhal, A V Rukmini, et al.
Neurology|April 27, 2011
Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMTJ Cassereau, C Casasnovas, N Gueguen, et al.
Pageof 15