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

A BOUE

Showing results (21-30 of 30) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 30 results.
Annales De Genetique|January 1, 1990
Strategy for constructing somatic hybrids isolating the two derivative chromosomes in X;autosome translocations. Application to a female patient t(X;5) with Hunter syndromeP Couillin, E Le Guern, N Ravise, 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|July 1, 1993
First-trimester free beta (hCG) screening for Down syndromeJ N Macri, K Spencer, D Aitken, 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.
Clinical Genetics|February 1, 1989
Genetic heterogeneity between two clinical forms of cystic fibrosis evidenced by familial analysis and linked DNA probesE Mornet, B Simon-Bouy, J L Serre, et al.
Prenatal Diagnosis|July 1, 1989
Early prenatal diagnosis of 21-hydroxylase deficiency using amniotic fluid 17-hydroxyprogesterone determination and DNA probesM Raux-Demay, E Mornet, J Boue, et al.
Endocrinology|May 1, 1984
17 beta-Hydroxysteroid dehydrogenase activity in human breast epithelial cell and fibroblast culturesJ F Prud'homme, C Malet, A Gompel, et al.
Prenatal Diagnosis|October 1, 1994
Amniotic fluid digestive enzymes: diagnostic value in fetal gastrointestinal obstructionsF Muller, M Dommergues, Y Ville, et al.
The EMBO Journal|June 1, 1988
Isolation of a human gene with protein sequence similarity to human and murine int-1 and the Drosophila segment polarity mutant winglessB J Wainwright, P J Scambler, P Stanier, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Annales De Genetique|January 1, 1990
Strategy for constructing somatic hybrids isolating the two derivative chromosomes in X;autosome translocations. Application to a female patient t(X;5) with Hunter syndromeP Couillin, E Le Guern, N Ravise, 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|July 1, 1993
First-trimester free beta (hCG) screening for Down syndromeJ N Macri, K Spencer, D Aitken, 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.
Clinical Genetics|February 1, 1989
Genetic heterogeneity between two clinical forms of cystic fibrosis evidenced by familial analysis and linked DNA probesE Mornet, B Simon-Bouy, J L Serre, et al.
Prenatal Diagnosis|July 1, 1989
Early prenatal diagnosis of 21-hydroxylase deficiency using amniotic fluid 17-hydroxyprogesterone determination and DNA probesM Raux-Demay, E Mornet, J Boue, et al.
Endocrinology|May 1, 1984
17 beta-Hydroxysteroid dehydrogenase activity in human breast epithelial cell and fibroblast culturesJ F Prud'homme, C Malet, A Gompel, et al.
Prenatal Diagnosis|October 1, 1994
Amniotic fluid digestive enzymes: diagnostic value in fetal gastrointestinal obstructionsF Muller, M Dommergues, Y Ville, et al.
The EMBO Journal|June 1, 1988
Isolation of a human gene with protein sequence similarity to human and murine int-1 and the Drosophila segment polarity mutant winglessB J Wainwright, P J Scambler, P Stanier, et al.
Pageof 3