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B Simon-Bouy

Showing results (11-20 of 60) with videos related to

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Clinical Genetics|June 18, 1998
The intermediate alleles of the fragile X CGG repeat in patients with mental retardationE Mornet, C Chateau, B Simon-Bouy, et al.
Revue D'Epidemiologie Et De Sante Publique|July 24, 2003
[Towards an improved antenatal screening for cystic fibrosis]J-L Serre, J Feingold, B Simon-Bouy, et al.
Prenatal Diagnosis|April 1, 1991
Consequences of prenatal diagnosis of cystic fibrosis on the reproductive attitudes of parents of affected childrenJ Boué, F Muller, B Simon-Bouy, et al.
Human Genetics|April 1, 1996
Recurrent and unexpected segregation of the FMR1 CGG repeat in a family with fragile X syndromeE Mornet, C Chateau, A Taillandier, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
General cystic fibrosis mutations are usually missense mutations affecting two specific protein domains and associated with a specific RFLP marker haplotypeJ L Serre, E Mornet, B Simon-Bouy, et al.
Clinical Genetics|September 1, 1991
Nine mutations in the cystic fibrosis (CF) gene account for 80% of the CF chromosomes in French patientsB Simon-Bouy, E Mornet, J L Serre, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1991
[Fortuitous discovery in echography of an isolated fetal intra-abdominal hyperechogenic mass. 87 cases]F Muller, B Simon-Bouy, M C Aubry, et al.
Human Genetics|September 1, 1990
The cystic fibrosis delta F508 mutation in the French populationB Simon-Bouy, E Mornet, J L Serre, et al.
Lancet (London, England)|July 8, 1989
Genetic differences between cystic fibrosis with and without meconium ileusB Simon-Bouy, J L Serre, E Mornet, 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.
Pageof 6

Showing results (11-20 of 60) with videos related to

Sort By:
Pageof 6
Clinical Genetics|June 18, 1998
The intermediate alleles of the fragile X CGG repeat in patients with mental retardationE Mornet, C Chateau, B Simon-Bouy, et al.
Revue D'Epidemiologie Et De Sante Publique|July 24, 2003
[Towards an improved antenatal screening for cystic fibrosis]J-L Serre, J Feingold, B Simon-Bouy, et al.
Prenatal Diagnosis|April 1, 1991
Consequences of prenatal diagnosis of cystic fibrosis on the reproductive attitudes of parents of affected childrenJ Boué, F Muller, B Simon-Bouy, et al.
Human Genetics|April 1, 1996
Recurrent and unexpected segregation of the FMR1 CGG repeat in a family with fragile X syndromeE Mornet, C Chateau, A Taillandier, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
General cystic fibrosis mutations are usually missense mutations affecting two specific protein domains and associated with a specific RFLP marker haplotypeJ L Serre, E Mornet, B Simon-Bouy, et al.
Clinical Genetics|September 1, 1991
Nine mutations in the cystic fibrosis (CF) gene account for 80% of the CF chromosomes in French patientsB Simon-Bouy, E Mornet, J L Serre, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1991
[Fortuitous discovery in echography of an isolated fetal intra-abdominal hyperechogenic mass. 87 cases]F Muller, B Simon-Bouy, M C Aubry, et al.
Human Genetics|September 1, 1990
The cystic fibrosis delta F508 mutation in the French populationB Simon-Bouy, E Mornet, J L Serre, et al.
Lancet (London, England)|July 8, 1989
Genetic differences between cystic fibrosis with and without meconium ileusB Simon-Bouy, J L Serre, E Mornet, 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.
Pageof 6