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C Ferec

Showing results (21-30 of 103) with videos related to

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Gut|January 22, 2000
Strong evidence that the N21I substitution in the cationic trypsinogen gene causes disease in hereditary pancreatitisJ M Chen, B Mercier, C Ferec
The New England Journal of Medicine|July 15, 2000
Atopy and a mutation in the interleukin-4 receptor geneD Dupre, M P Audrezet, C Ferec
Tissue Antigens|August 1, 1992
Improvement in HLA-DQB typing by PCR-RFLP: introduction of a constant restriction site in one of the primers for digestion controlB Mercier, C Ferec, F Dufosse, et al.
Journal of Medical Genetics|September 1, 1992
A mutation in exon 7 of the CFTR gene is common in the western part of FranceM P Audrezet, B Mercier, H Guillermit, et al.
Gastroenterologie Clinique Et Biologique|January 1, 1994
[Changes in the TP53 tumor suppressor gene in malignant transformation of Barrett esophagus]C Ferec, M P Audrezet, B Mercier, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1988
[Prenatal diagnosis of mucoviscidosis. Contribution of DNA analysis of trophoblast biopsies]C Ferec, J J Chabaud, P Parent, et al.
Human Mutation|June 22, 2000
Identification of 3 novel mutations (Y4236X, Q3820X, 11745+2 ins3) in autosomal dominant polycystic kidney disease 1 gene (PKD1)R Perrichot, B Mercier, A Carre, et al.
Pathologie-Biologie|October 14, 1998
TP53 and oesophageal cancerC Ferec, M A Giroux, M P Audrezet, et al.
Journal De Genetique Humaine|June 1, 1989
[Analysis of 112 haplotypes carrying the cystic fibrosis gene. Applications in genetic counseling]P Parent, C Ferec, J F Morin, et al.
Journal of Medical Genetics|February 26, 2000
Mutational analysis of the human pancreatic secretory trypsin inhibitor (PSTI) gene in hereditary and sporadic chronic pancreatitisJ M Chen, B Mercier, M P Audrezet, et al.
Pageof 11

Showing results (21-30 of 103) with videos related to

Sort By:
Pageof 11
Gut|January 22, 2000
Strong evidence that the N21I substitution in the cationic trypsinogen gene causes disease in hereditary pancreatitisJ M Chen, B Mercier, C Ferec
The New England Journal of Medicine|July 15, 2000
Atopy and a mutation in the interleukin-4 receptor geneD Dupre, M P Audrezet, C Ferec
Tissue Antigens|August 1, 1992
Improvement in HLA-DQB typing by PCR-RFLP: introduction of a constant restriction site in one of the primers for digestion controlB Mercier, C Ferec, F Dufosse, et al.
Journal of Medical Genetics|September 1, 1992
A mutation in exon 7 of the CFTR gene is common in the western part of FranceM P Audrezet, B Mercier, H Guillermit, et al.
Gastroenterologie Clinique Et Biologique|January 1, 1994
[Changes in the TP53 tumor suppressor gene in malignant transformation of Barrett esophagus]C Ferec, M P Audrezet, B Mercier, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1988
[Prenatal diagnosis of mucoviscidosis. Contribution of DNA analysis of trophoblast biopsies]C Ferec, J J Chabaud, P Parent, et al.
Human Mutation|June 22, 2000
Identification of 3 novel mutations (Y4236X, Q3820X, 11745+2 ins3) in autosomal dominant polycystic kidney disease 1 gene (PKD1)R Perrichot, B Mercier, A Carre, et al.
Pathologie-Biologie|October 14, 1998
TP53 and oesophageal cancerC Ferec, M A Giroux, M P Audrezet, et al.
Journal De Genetique Humaine|June 1, 1989
[Analysis of 112 haplotypes carrying the cystic fibrosis gene. Applications in genetic counseling]P Parent, C Ferec, J F Morin, et al.
Journal of Medical Genetics|February 26, 2000
Mutational analysis of the human pancreatic secretory trypsin inhibitor (PSTI) gene in hereditary and sporadic chronic pancreatitisJ M Chen, B Mercier, M P Audrezet, et al.
Pageof 11