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

P Parent

Showing results (81-90 of 86) with videos related to

Pageof 9
Sort By:
You have reached the last page of results.This site can display upto 86 results.
Clinical Genetics|February 13, 2001
Prevalence of CFTR mutations in hypertrypsinaemia detected through neonatal screening for cystic fibrosisV Scotet, M De Braekeleer, M P Audrézet, et al.
American Journal of Human Genetics|November 11, 1992
DNA polymorphism analysis in families with recurrence of free trisomy 21C G Pangalos, C C Talbot, J G Lewis, et al.
Journal of Medical Genetics|April 6, 2001
Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardationF Giraudeau, L Taine, V Biancalana, et al.
Lancet (London, England)|October 7, 2000
Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosisV Scotet, M de Braekeleer, M Roussey, et al.
Journal of Medical Genetics|January 7, 2006
Clinical, molecular, and genotype-phenotype correlation studies from 25 cases of oral-facial-digital syndrome type 1: a French and Belgian collaborative studyC Thauvin-Robinet, M Cossée, V Cormier-Daire, et al.
Scientific Reports|November 25, 2016
First in-flight synchrotron X-ray absorption and photoemission study of carbon soot nanoparticlesF-X Ouf, P Parent, C Laffon, et al.
Pageof 9

Showing results (81-90 of 86) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 86 results.
Clinical Genetics|February 13, 2001
Prevalence of CFTR mutations in hypertrypsinaemia detected through neonatal screening for cystic fibrosisV Scotet, M De Braekeleer, M P Audrézet, et al.
American Journal of Human Genetics|November 11, 1992
DNA polymorphism analysis in families with recurrence of free trisomy 21C G Pangalos, C C Talbot, J G Lewis, et al.
Journal of Medical Genetics|April 6, 2001
Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardationF Giraudeau, L Taine, V Biancalana, et al.
Lancet (London, England)|October 7, 2000
Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosisV Scotet, M de Braekeleer, M Roussey, et al.
Journal of Medical Genetics|January 7, 2006
Clinical, molecular, and genotype-phenotype correlation studies from 25 cases of oral-facial-digital syndrome type 1: a French and Belgian collaborative studyC Thauvin-Robinet, M Cossée, V Cormier-Daire, et al.
Scientific Reports|November 25, 2016
First in-flight synchrotron X-ray absorption and photoemission study of carbon soot nanoparticlesF-X Ouf, P Parent, C Laffon, et al.
Pageof 9