Characterisation of 98 alleles in 105 unrelated individuals in the F8VWF gene.

Por Mercier, B, Gaucher, C, Mazurier, C
Publicado em 1991

An MspI polymorphism in the von Willebrand Factor gene

Por Mercier, B., Gaucher, C., Mazurier, C.
Publicado em 1990

Strong evidence that the N21I substitution in the cationic trypsinogen gene causes disease in hereditary pancreatitis

Por CHEN, J, MERCIER, B, FEREC, C
Publicado em 1999

Basal ganglia and cerebellum receive different somatosensory information in rats.

Por Mercier, B E, Legg, C R, Glickstein, M
Publicado em 1990

Direct PCR from whole blood, without DNA extraction.

Por Mercier, B, Gaucher, C, Feugeas, O, Mazurier, C
Publicado em 1990

Mutational analysis of the human pancreatic secretory trypsin inhibitor (PSTI) gene in hereditary and sporadic chronic pancreatitis

Por CHEN, J., MERCIER, B., AUDREZET, M., FEREC, C.
Publicado em 2000

A mutation in exon 7 of the CFTR gene is common in the western part of France.

Por Audrezet, M P, Mercier, B, Guillermit, H, Ferec, C
Publicado em 1992

Monte-Carlo methods and applications in neutronics, photonics and statistical physics : proceedings of the joint los Alamos National Laboratory commissariat à l'energie atomique me...

Por Forster, A., Ledanois, G., Mercier, B., Alcouffe, R., Dautray, R.
Publicado em 1985

A polymorphism in intron 20 of the CFTR gene

Por Quere, I., Guillermit, H., Mercier, B., Audrezet, M.P., Ferec, C.
Publicado em 1991

Absence of mutations in the interspecies conserved regions of the CFTR promoter region in cystic fibrosis (CF) and CF related patients.

Por Verlingue, C, Vuillaumier, S, Mercier, B, Le Gac, M, Elion, J, Férec, C, Denamur, E
Publicado em 1998

Mild pulmonary, but severe hepatic disease in a cystic fibrosis patient homozygous for a frameshift mutation in the regulatory domain of the CFTR.

Por Lissens, W, Desmyttere, S, Bonduelle, M, Dab, I, Liebaers, I, Mercier, B, Audrezet, M P, Ferec, C
Publicado em 1993

Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patients.

Por Mercier, B, Verlingue, C, Lissens, W, Silber, S J, Novelli, G, Bonduelle, M, Audrézet, M P, Férec, C
Publicado em 1995

Prenatal detection of cystic fibrosis by ultrasonography: a retrospective study of more than 346 000 pregnancies

Por Scotet, V, De Braekeleer, M, Audrezet, M, Quere, I, Mercier, B, Dugueperoux, I, Andrieux, J, Blayau, M, Ferec, C
Publicado em 2002

Association of 1078 del T cystic fibrosis mutation with severe disease.

Por Moullier, P, Jéhanne, M, Audrézet, M P, Mercier, B, Verlingue, C, Quéré, I, Guillermit, H, Raguénès, O, Storni, V, Rault, G
Publicado em 1994

A cluster of cystic fibrosis mutations in exon 17b of the CFTR gene: a site for rare mutations.

Por Mercier, B, Lissens, W, Novelli, G, Kalaydjieva, L, de Arce, M, Kapranov, N, Canki Klain, N, Estivill, X, Palacio, A, Cashman, S
Publicado em 1994

Mutations in the cationic trypsinogen gene and evidence for genetic heterogeneity in hereditary pancreatitis

Por Ferec, C, Raguenes, O, Salomon, R, Roche, C, Bernard, J, Guillot, M, Quere, I, Faure, C, Mercier, B, Audrezet, M, Guillausseau, P, Dupont, C, Munnich, A, Bignon, J, Le Bodic, L
Publicado em 1999