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Gut
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January 22, 2000
Strong evidence that the N21I substitution in the cationic trypsinogen gene causes disease in hereditary pancreatitis
J M Chen, B Mercier, C Ferec
The New England Journal of Medicine
|
July 15, 2000
Atopy and a mutation in the interleukin-4 receptor gene
D 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 control
B 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 France
M 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 cancer
C 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 pancreatitis
J M Chen, B Mercier, M P Audrezet, et al.
Page
of 11
Search research articles
Search
Showing results (21-30 of 103) with videos related to
Sort By:
Page
of 11
Gut
|
January 22, 2000
Strong evidence that the N21I substitution in the cationic trypsinogen gene causes disease in hereditary pancreatitis
J M Chen, B Mercier, C Ferec
The New England Journal of Medicine
|
July 15, 2000
Atopy and a mutation in the interleukin-4 receptor gene
D 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 control
B 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 France
M 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 cancer
C 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 pancreatitis
J M Chen, B Mercier, M P Audrezet, et al.
Page
of 11