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E Girodon

Showing results (1-10 of 54) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 17, 2020
PrefaceE Girodon, I Fajac
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 17, 2020
Genomically-guided therapies: A new era for cystic fibrosisI Fajac, E Girodon
Journal of the International Federation of Clinical Chemistry|March 9, 1995
Prenatal diagnosis of hemoglobinopathiesE Girodon, N Ghanem, M Goossens
Human Mutation|January 29, 2000
Screening practices for mutations in the CFTR gene ABCC7E Girodon-Boulandet, C Cazeneuve, M Goossens
Revue De Pneumologie Clinique|January 1, 1995
[Cystic fibrosis: the CFTR gene, its mutations, the genetic counseling]M Goossens, N Ghanem, E Girodon, et al.
Prenatal Diagnosis|February 1, 1996
PK Mondor: prenatal diagnosis of a frameshift mutation in the LR pyruvate kinase gene associated with severe hereditary non-spherocytic haemolytic anaemiaH Rouger, E Girodon, M Goossens, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|October 26, 1999
Lack of evidence of heterozygosity for cystic fibrosis as a risk factor for invasive aspergillosis in haematological patientsB Costes, E Girodon, L Jabot-Lestang, et al.
Journal of Medical Genetics|August 3, 2000
Fetal bowel hyperechogenicity may indicate mild atypical cystic fibrosis: a case associated with a complex CFTR alleleM J Abramowicz, B Dessars, C Sevens, et al.
Genomics|May 15, 1994
Identification of eight mutations and three sequence variations in the cystic fibrosis transmembrane conductance regulator (CFTR) geneN Ghanem, B Costes, E Girodon, et al.
Clinical Genetics|August 18, 1999
Determination of the prevalence of cystic fibrosis in the United Arab Emirates by genetic carrier screeningP M Frossard, G Lestringant, E Girodon, et al.
Pageof 6

Showing results (1-10 of 54) with videos related to

Sort By:
Pageof 6
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 17, 2020
PrefaceE Girodon, I Fajac
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 17, 2020
Genomically-guided therapies: A new era for cystic fibrosisI Fajac, E Girodon
Journal of the International Federation of Clinical Chemistry|March 9, 1995
Prenatal diagnosis of hemoglobinopathiesE Girodon, N Ghanem, M Goossens
Human Mutation|January 29, 2000
Screening practices for mutations in the CFTR gene ABCC7E Girodon-Boulandet, C Cazeneuve, M Goossens
Revue De Pneumologie Clinique|January 1, 1995
[Cystic fibrosis: the CFTR gene, its mutations, the genetic counseling]M Goossens, N Ghanem, E Girodon, et al.
Prenatal Diagnosis|February 1, 1996
PK Mondor: prenatal diagnosis of a frameshift mutation in the LR pyruvate kinase gene associated with severe hereditary non-spherocytic haemolytic anaemiaH Rouger, E Girodon, M Goossens, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|October 26, 1999
Lack of evidence of heterozygosity for cystic fibrosis as a risk factor for invasive aspergillosis in haematological patientsB Costes, E Girodon, L Jabot-Lestang, et al.
Journal of Medical Genetics|August 3, 2000
Fetal bowel hyperechogenicity may indicate mild atypical cystic fibrosis: a case associated with a complex CFTR alleleM J Abramowicz, B Dessars, C Sevens, et al.
Genomics|May 15, 1994
Identification of eight mutations and three sequence variations in the cystic fibrosis transmembrane conductance regulator (CFTR) geneN Ghanem, B Costes, E Girodon, et al.
Clinical Genetics|August 18, 1999
Determination of the prevalence of cystic fibrosis in the United Arab Emirates by genetic carrier screeningP M Frossard, G Lestringant, E Girodon, et al.
Pageof 6