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

G van Camp

Showing results (131-140 of 214) with videos related to

Pageof 22
Sort By:
Circulation|July 27, 2001
Destruction of contrast microbubbles by ultrasound: effects on myocardial function, coronary perfusion pressure, and microvascular integrityT Ay, X Havaux, G Van Camp, et al.
Gastroenterologie Clinique Et Biologique|January 1, 1997
[Mutations of the endothelin-3 gene in isolated and syndromic forms of Hirschsprung disease]C Bidaud, R Salomon, P Edery, et al.
Microbial Genomics|March 7, 2022
Population structure of ocular <i>Streptococcus pneumoniae</i> is highly diverse and formed by lineages that escape current vaccinesCamille Andre, John Rouhana, Suelen Scarpa de Mello, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
Multiple origins of the mtDNA 7472insC mutation associated with hearing loss and neurological dysfunctionT P Hutchin, N C Navarro-Coy, G Van Camp, et al.
American Journal of Medical Genetics. Supplement|January 1, 1990
Study of the origin of nondisjunction in a family with two cases of Down syndrome using cytogenetic and molecular polymorphismsP Stinissen, B Van Roy, G Van Camp, et al.
Nature Genetics|July 1, 1994
MASA syndrome is due to mutations in the neural cell adhesion gene L1CAML Vits, G Van Camp, P Coucke, et al.
Genetic Testing|October 24, 2007
A new, easy, and rapid high-throughput detection method for the common GJB2 (CX26), 35delG mutationE Van Eyken, G Van Camp, J J Hendrickx, et al.
Genomics|March 1, 1993
A contiguous physical map of the pericentromeric region of chromosome 21q between D21Z1 and D21S13EW Van Hul, G Van Camp, L Stuyver, et al.
Human Molecular Genetics|September 1, 1995
Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14qK Fukushima, A Ramesh, C R Srisailapathy, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|April 28, 2017
Primary tumor sidedness has an impact on prognosis and treatment outcome in metastatic colorectal cancer: results from two randomized first-line panitumumab studiesN Boeckx, R Koukakis, K Op de Beeck, et al.
Pageof 22

Showing results (131-140 of 214) with videos related to

Sort By:
Pageof 22
Circulation|July 27, 2001
Destruction of contrast microbubbles by ultrasound: effects on myocardial function, coronary perfusion pressure, and microvascular integrityT Ay, X Havaux, G Van Camp, et al.
Gastroenterologie Clinique Et Biologique|January 1, 1997
[Mutations of the endothelin-3 gene in isolated and syndromic forms of Hirschsprung disease]C Bidaud, R Salomon, P Edery, et al.
Microbial Genomics|March 7, 2022
Population structure of ocular <i>Streptococcus pneumoniae</i> is highly diverse and formed by lineages that escape current vaccinesCamille Andre, John Rouhana, Suelen Scarpa de Mello, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
Multiple origins of the mtDNA 7472insC mutation associated with hearing loss and neurological dysfunctionT P Hutchin, N C Navarro-Coy, G Van Camp, et al.
American Journal of Medical Genetics. Supplement|January 1, 1990
Study of the origin of nondisjunction in a family with two cases of Down syndrome using cytogenetic and molecular polymorphismsP Stinissen, B Van Roy, G Van Camp, et al.
Nature Genetics|July 1, 1994
MASA syndrome is due to mutations in the neural cell adhesion gene L1CAML Vits, G Van Camp, P Coucke, et al.
Genetic Testing|October 24, 2007
A new, easy, and rapid high-throughput detection method for the common GJB2 (CX26), 35delG mutationE Van Eyken, G Van Camp, J J Hendrickx, et al.
Genomics|March 1, 1993
A contiguous physical map of the pericentromeric region of chromosome 21q between D21Z1 and D21S13EW Van Hul, G Van Camp, L Stuyver, et al.
Human Molecular Genetics|September 1, 1995
Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14qK Fukushima, A Ramesh, C R Srisailapathy, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|April 28, 2017
Primary tumor sidedness has an impact on prognosis and treatment outcome in metastatic colorectal cancer: results from two randomized first-line panitumumab studiesN Boeckx, R Koukakis, K Op de Beeck, et al.
Pageof 22