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

F R VARGAS

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

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 20 results.
Journal of Clinical Pathology|May 29, 2004
Identification of three novel RB1 mutations in Brazilian patients with retinoblastoma by "exon by exon" PCR mediated SSCP analysisE Braggio, C R Bonvicino, F R Vargas, et al.
Journal of Medical Genetics|January 1, 1995
Further report of a patient with humeroradioulnar synostosis and hydronephrosisR Boy, D Horovitz, F R Vargas, et al.
American Journal of Medical Genetics|July 17, 1995
Autosomal dominant osteosclerosis type Stanescu: the third familyD D Horovitz, J G Barbosa Neto, R Boy, et al.
Pediatric Blood & Cancer|September 17, 2013
Association of TP53 polymorphisms on the risk of Wilms tumorR C Andrade, L C A Cardoso, S E Ferman, et al.
Cancer Genetics and Cytogenetics|June 19, 2008
Founder effect of the BRCA1 5382insC mutation in Brazilian patients with hereditary breast ovary cancer syndromeE C B da Costa, F R Vargas, A S Moreira, et al.
Human Genetics|January 1, 1996
Xp-duplications with and without sex reversalA Baumstark, G Barbi, M Djalali, et al.
American Journal of Medical Genetics|August 1, 1993
Limb deficiency with or without Möbius sequence in seven Brazilian children associated with misoprostol use in the first trimester of pregnancyC H Gonzalez, F R Vargas, A B Perez, et al.
American Journal of Medical Genetics|February 24, 2001
Prenatal exposure to misoprostol and vascular disruption defects: a case-control studyF R Vargas, L Schuler-Faccini, D Brunoni, et al.
Human Genetics|May 26, 1998
Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactylyF R Vargas, E Roessler, K Gaudenz, et al.
Clinical Genetics|October 10, 2013
Huntington disease and Huntington disease-like in a case series from BrazilR M Castilhos, A F D Souza, G V Furtado, et al.
Pageof 2

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

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Journal of Clinical Pathology|May 29, 2004
Identification of three novel RB1 mutations in Brazilian patients with retinoblastoma by "exon by exon" PCR mediated SSCP analysisE Braggio, C R Bonvicino, F R Vargas, et al.
Journal of Medical Genetics|January 1, 1995
Further report of a patient with humeroradioulnar synostosis and hydronephrosisR Boy, D Horovitz, F R Vargas, et al.
American Journal of Medical Genetics|July 17, 1995
Autosomal dominant osteosclerosis type Stanescu: the third familyD D Horovitz, J G Barbosa Neto, R Boy, et al.
Pediatric Blood & Cancer|September 17, 2013
Association of TP53 polymorphisms on the risk of Wilms tumorR C Andrade, L C A Cardoso, S E Ferman, et al.
Cancer Genetics and Cytogenetics|June 19, 2008
Founder effect of the BRCA1 5382insC mutation in Brazilian patients with hereditary breast ovary cancer syndromeE C B da Costa, F R Vargas, A S Moreira, et al.
Human Genetics|January 1, 1996
Xp-duplications with and without sex reversalA Baumstark, G Barbi, M Djalali, et al.
American Journal of Medical Genetics|August 1, 1993
Limb deficiency with or without Möbius sequence in seven Brazilian children associated with misoprostol use in the first trimester of pregnancyC H Gonzalez, F R Vargas, A B Perez, et al.
American Journal of Medical Genetics|February 24, 2001
Prenatal exposure to misoprostol and vascular disruption defects: a case-control studyF R Vargas, L Schuler-Faccini, D Brunoni, et al.
Human Genetics|May 26, 1998
Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactylyF R Vargas, E Roessler, K Gaudenz, et al.
Clinical Genetics|October 10, 2013
Huntington disease and Huntington disease-like in a case series from BrazilR M Castilhos, A F D Souza, G V Furtado, et al.
Pageof 2