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

E Legius

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

Pageof 12
Sort By:
You have reached the last page of results.This site can display upto 120 results.
American Journal of Medical Genetics. Part A|February 28, 2003
Personality profiles of children and adolescents with neurofibromatosis type 1P Prinzie, M J Descheemaeker, A Vogels, et al.
Human Molecular Genetics|July 7, 2001
Recombination hotspot in NF1 microdeletion patientsC López-Correa, M Dorschner, H Brems, et al.
British Journal of Cancer|March 15, 2012
Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer familiesD J Osher, K De Leeneer, G Michils, et al.
Nature Genetics|February 14, 1998
SOX10 mutations in patients with Waardenburg-Hirschsprung diseaseV Pingault, N Bondurand, K Kuhlbrodt, et al.
Journal of Medical Genetics|June 10, 2005
Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGHK K Mantripragada, A-C Thuresson, A Piotrowski, et al.
American Journal of Human Genetics|April 29, 1998
Mutation analysis of patients with Hermansky-Pudlak syndrome: a frameshift hot spot in the HPS gene and apparent locus heterogeneityJ Oh, L Ho, S Ala-Mello, et al.
Nature Genetics|September 2, 1999
Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasiaJ R Hurvitz, W M Suwairi, W Van Hul, et al.
Community Genetics|August 28, 2004
Cancer genetics service provision: a comparison of seven European centresP Hopwood, C J van Asperen, G Borreani, et al.
Breast Cancer Research and Treatment|February 29, 2012
Evaluation of RAD51C as cancer susceptibility gene in a large breast-ovarian cancer patient population referred for genetic testingK De Leeneer, M Van Bockstal, S De Brouwer, et al.
Science (New York, N.Y.)|November 17, 2018
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitinationM Steklov, S Pandolfi, M F Baietti, et al.
Pageof 12

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

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 120 results.
American Journal of Medical Genetics. Part A|February 28, 2003
Personality profiles of children and adolescents with neurofibromatosis type 1P Prinzie, M J Descheemaeker, A Vogels, et al.
Human Molecular Genetics|July 7, 2001
Recombination hotspot in NF1 microdeletion patientsC López-Correa, M Dorschner, H Brems, et al.
British Journal of Cancer|March 15, 2012
Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer familiesD J Osher, K De Leeneer, G Michils, et al.
Nature Genetics|February 14, 1998
SOX10 mutations in patients with Waardenburg-Hirschsprung diseaseV Pingault, N Bondurand, K Kuhlbrodt, et al.
Journal of Medical Genetics|June 10, 2005
Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGHK K Mantripragada, A-C Thuresson, A Piotrowski, et al.
American Journal of Human Genetics|April 29, 1998
Mutation analysis of patients with Hermansky-Pudlak syndrome: a frameshift hot spot in the HPS gene and apparent locus heterogeneityJ Oh, L Ho, S Ala-Mello, et al.
Nature Genetics|September 2, 1999
Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasiaJ R Hurvitz, W M Suwairi, W Van Hul, et al.
Community Genetics|August 28, 2004
Cancer genetics service provision: a comparison of seven European centresP Hopwood, C J van Asperen, G Borreani, et al.
Breast Cancer Research and Treatment|February 29, 2012
Evaluation of RAD51C as cancer susceptibility gene in a large breast-ovarian cancer patient population referred for genetic testingK De Leeneer, M Van Bockstal, S De Brouwer, et al.
Science (New York, N.Y.)|November 17, 2018
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitinationM Steklov, S Pandolfi, M F Baietti, et al.
Pageof 12