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

J Boue

Showing results (11-20 of 27) with videos related to

Pageof 3
Sort By:
Human Genetics|January 1, 1984
The gene for human fibroblast interferon (IFB) maps to 9p21L Henry, J Sizun, C Turleau, et al.
Fetal Diagnosis and Therapy|January 1, 1993
Prenatal diagnosis of cystic fibrosis: ultrasonography of the gallbladder at 17-19 weeks of gestationF Duchatel, F Muller, J F Oury, et al.
Clinical Genetics|November 1, 1976
Prenatal diagnosis of fucosidosisL Poenaru, J C Dreyfus, J Boue, et al.
Prenatal Diagnosis|May 1, 1987
Prenatal diagnosis of chronic granulomatous disease (CGD) in four high risk male fetusesT P Huu, Y Dumez, C Marquetty, et al.
Prenatal Diagnosis|April 1, 1990
Prenatal diagnosis of mucolipidosis type II on first-trimester amniotic fluidL Poenaru, C Mezard, S Akli, et al.
Clinical Genetics|April 1, 1991
The delta F508 mutation in mild adult forms of cystic fibrosis (CF)B Simon-Bouy, E Mornet, A Taillandier, et al.
Human Genetics|January 1, 1983
Evidence for the presence of beta-subunit of hexosaminidase in a case of Sandhoff disease using a blotting techniqueS Gautron, L Poenaru, J Boue, et al.
Human Genetics|February 1, 1992
Carrier detection and prenatal diagnosis of cystic fibrosis using an intragenic TA-repeat polymorphismE Mornet, C Chateau, B Simon-Bouy, et al.
Prenatal Diagnosis|January 1, 1981
Prenatal diagnosis of congenital enzymopenic methaemoglobinaemia with mental retardation due to generalized cytochrome b5 reductase deficiency: first report of two casesC Junien, A Leroux, D Lostanlen, et al.
Lancet (London, England)|February 20, 1988
Genetic differences between cystic fibrosis with and without meconium ileusE Mornet, B Simon-Bouy, J L Serre, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Human Genetics|January 1, 1984
The gene for human fibroblast interferon (IFB) maps to 9p21L Henry, J Sizun, C Turleau, et al.
Fetal Diagnosis and Therapy|January 1, 1993
Prenatal diagnosis of cystic fibrosis: ultrasonography of the gallbladder at 17-19 weeks of gestationF Duchatel, F Muller, J F Oury, et al.
Clinical Genetics|November 1, 1976
Prenatal diagnosis of fucosidosisL Poenaru, J C Dreyfus, J Boue, et al.
Prenatal Diagnosis|May 1, 1987
Prenatal diagnosis of chronic granulomatous disease (CGD) in four high risk male fetusesT P Huu, Y Dumez, C Marquetty, et al.
Prenatal Diagnosis|April 1, 1990
Prenatal diagnosis of mucolipidosis type II on first-trimester amniotic fluidL Poenaru, C Mezard, S Akli, et al.
Clinical Genetics|April 1, 1991
The delta F508 mutation in mild adult forms of cystic fibrosis (CF)B Simon-Bouy, E Mornet, A Taillandier, et al.
Human Genetics|January 1, 1983
Evidence for the presence of beta-subunit of hexosaminidase in a case of Sandhoff disease using a blotting techniqueS Gautron, L Poenaru, J Boue, et al.
Human Genetics|February 1, 1992
Carrier detection and prenatal diagnosis of cystic fibrosis using an intragenic TA-repeat polymorphismE Mornet, C Chateau, B Simon-Bouy, et al.
Prenatal Diagnosis|January 1, 1981
Prenatal diagnosis of congenital enzymopenic methaemoglobinaemia with mental retardation due to generalized cytochrome b5 reductase deficiency: first report of two casesC Junien, A Leroux, D Lostanlen, et al.
Lancet (London, England)|February 20, 1988
Genetic differences between cystic fibrosis with and without meconium ileusE Mornet, B Simon-Bouy, J L Serre, et al.
Pageof 3