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C Petit

Showing results (351-360 of 563) with videos related to

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Infection|January 1, 1994
Skin versus hub cultures to predict colonization and infection of central venous catheter in intensive care patientsB Guidet, I Nicola, V Barakett, et al.
Brain : a Journal of Neurology|June 1, 1994
Right frontal cortex hypometabolism in transient global amnesia. A PET studyJ C Baron, M C Petit-Taboué, F Le Doze, et al.
American Journal of Medical Genetics|June 8, 2001
From DFNB2 to Usher syndrome: variable expressivity of the same diseaseZ B Zina, S Masmoudi, H Ayadi, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Deletion of the pseudoautosomal region and lack of sex-chromosome pairing at pachytene in two infertile men carrying an X;Y translocationO Gabriel-Robez, Y Rumpler, C Ratomponirina, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 23, 2012
[Hepatic alveolar echinococcosis: a rare cause of recurrent, surgically curable abdominal pain in children]C Guinet, E Guiot, G De Miscault, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|July 4, 2006
First cluster of C. difficile toxinotype III, PCR-ribotype 027 associated disease in France: preliminary reportM Tachon, C Cattoen, K Blanckaert, et al.
European Journal of Human Genetics : EJHG|July 1, 1997
BOR and BO syndromes are allelic defects of EYA1C Vincent, V Kalatzis, S Abdelhak, et al.
Pathologie-Biologie|December 15, 2004
[Totally implantable venous access ports: frequency of complications and analysis of bacterial contamination after ablation]F Barbut, S Soukouna, V Lalande, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36M Mustapha, S Chardenoux, A Nieder, et al.
Archives of Otolaryngology--Head & Neck Surgery|September 5, 2001
Connexin 26 gene mutations in congenitally deaf children: pitfalls for genetic counselingS Marlin, E N Garabédian, G Roger, et al.
Pageof 57

Showing results (351-360 of 563) with videos related to

Sort By:
Pageof 57
Infection|January 1, 1994
Skin versus hub cultures to predict colonization and infection of central venous catheter in intensive care patientsB Guidet, I Nicola, V Barakett, et al.
Brain : a Journal of Neurology|June 1, 1994
Right frontal cortex hypometabolism in transient global amnesia. A PET studyJ C Baron, M C Petit-Taboué, F Le Doze, et al.
American Journal of Medical Genetics|June 8, 2001
From DFNB2 to Usher syndrome: variable expressivity of the same diseaseZ B Zina, S Masmoudi, H Ayadi, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Deletion of the pseudoautosomal region and lack of sex-chromosome pairing at pachytene in two infertile men carrying an X;Y translocationO Gabriel-Robez, Y Rumpler, C Ratomponirina, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 23, 2012
[Hepatic alveolar echinococcosis: a rare cause of recurrent, surgically curable abdominal pain in children]C Guinet, E Guiot, G De Miscault, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|July 4, 2006
First cluster of C. difficile toxinotype III, PCR-ribotype 027 associated disease in France: preliminary reportM Tachon, C Cattoen, K Blanckaert, et al.
European Journal of Human Genetics : EJHG|July 1, 1997
BOR and BO syndromes are allelic defects of EYA1C Vincent, V Kalatzis, S Abdelhak, et al.
Pathologie-Biologie|December 15, 2004
[Totally implantable venous access ports: frequency of complications and analysis of bacterial contamination after ablation]F Barbut, S Soukouna, V Lalande, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36M Mustapha, S Chardenoux, A Nieder, et al.
Archives of Otolaryngology--Head & Neck Surgery|September 5, 2001
Connexin 26 gene mutations in congenitally deaf children: pitfalls for genetic counselingS Marlin, E N Garabédian, G Roger, et al.
Pageof 57