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La Revue Du Praticien
|
January 1, 1985
[Duodenopancreatic contusions]
J C Patel, D Baux
Chirurgie Pediatrique
|
January 1, 1980
[Esophageal atresia and gastro-esophageal reflux]
F Gauthier, O Gaudiche, D Baux, et al.
Presse Medicale (Paris, France : 1983)
|
June 27, 1987
[Post-traumatic hemobilia. Is selective hepatic artery ligation dangerous?]
T Yandza, G Fourtanier, D Baux, et al.
La Nouvelle Presse Medicale
|
March 7, 1981
[Echotomographic diagnosis of multiple abscesses of the kidney]
A Legros, D Baux, J Leclère, et al.
Biochemical and Biophysical Research Communications
|
August 7, 2007
First functional polymorphism in CFTR promoter that results in decreased transcriptional activity and Sp1/USF binding
M Taulan, E Lopez, C Guittard, et al.
Clinical Genetics
|
September 8, 2011
Audiological findings in 100 USH2 patients
C Abadie, C Blanchet, D Baux, et al.
Pathologie-Biologie
|
December 4, 2009
[Genetic mutation databases: stakes and perspectives for orphan genetic diseases]
V Humbertclaude, S Tuffery-Giraud, C Bareil, et al.
Scientific Reports
|
December 3, 2017
Combined genetic approaches yield a 48% diagnostic rate in a large cohort of French hearing-impaired patients
D Baux, C Vaché, C Blanchet, et al.
Scientific Reports
|
July 6, 2022
Noninvasive prenatal diagnosis of genetic diseases induced by triplet repeat expansion by linked read haplotyping and Bayesian approach
C Liautard-Haag, G Durif, C VanGoethem, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
La Revue Du Praticien
|
January 1, 1985
[Duodenopancreatic contusions]
J C Patel, D Baux
Chirurgie Pediatrique
|
January 1, 1980
[Esophageal atresia and gastro-esophageal reflux]
F Gauthier, O Gaudiche, D Baux, et al.
Presse Medicale (Paris, France : 1983)
|
June 27, 1987
[Post-traumatic hemobilia. Is selective hepatic artery ligation dangerous?]
T Yandza, G Fourtanier, D Baux, et al.
La Nouvelle Presse Medicale
|
March 7, 1981
[Echotomographic diagnosis of multiple abscesses of the kidney]
A Legros, D Baux, J Leclère, et al.
Biochemical and Biophysical Research Communications
|
August 7, 2007
First functional polymorphism in CFTR promoter that results in decreased transcriptional activity and Sp1/USF binding
M Taulan, E Lopez, C Guittard, et al.
Clinical Genetics
|
September 8, 2011
Audiological findings in 100 USH2 patients
C Abadie, C Blanchet, D Baux, et al.
Pathologie-Biologie
|
December 4, 2009
[Genetic mutation databases: stakes and perspectives for orphan genetic diseases]
V Humbertclaude, S Tuffery-Giraud, C Bareil, et al.
Scientific Reports
|
December 3, 2017
Combined genetic approaches yield a 48% diagnostic rate in a large cohort of French hearing-impaired patients
D Baux, C Vaché, C Blanchet, et al.
Scientific Reports
|
July 6, 2022
Noninvasive prenatal diagnosis of genetic diseases induced by triplet repeat expansion by linked read haplotyping and Bayesian approach
C Liautard-Haag, G Durif, C VanGoethem, et al.
Page
of 1