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Showing results (61-70 of 79) with videos related to

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Pathologie-Biologie|October 14, 1998
[Interest of gene amplification by PCR for the diagnosis of Mycoplasma pneumoniae infections in the child]F Grattard, T Bourlet, C Galambrun, et al.
Journal De Genetique Humaine|March 1, 1981
[Early clinical and histopathological manifestations in 14 boys showing elevated serum creatine-phosphokinase levels in their first year]P Guibaud, H N Carrier, H Plauchu, et al.
Journal of Clinical Microbiology|March 1, 1994
Arbitrarily primed PCR, ribotyping, and plasmid pattern analysis applied to investigation of a nosocomial outbreak due to Enterobacter cloacae in a neonatal intensive care unitF Grattard, B Pozzetto, P Berthelot, et al.
Annales De Genetique|January 1, 1981
[Partial monosomy 20q: a new syndrome. Regional assignment of the adenosine deaminase (ADA) locus on 20q132 (author's transl)]J Fraisse, M F Bertheas, F Frère, et al.
Pediatrie|July 1, 1975
[Aseptic osteonecrosis following corticoid therapy and immunodepressive agents in children. Apropos of 3 observations]G Korkmaz, M David, B Parchoux, et al.
Journal De Genetique Humaine|March 1, 1979
[The present status of the chromosome map of man. I. Methods]T Philip, J Fraisse, P Guibaud, et al.
Gynecologie, Obstetrique & Fertilite|January 23, 2004
[A simple, low-cost and non-invasive method for screening Y microdeletions in infertile men]I Aknin-Seifer, R-L Touraine, H Lejeune, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|June 3, 1982
[Partial monosomy 20q : a new syndrome. Regional assignment of the ADA locus on 20q132 (author's transl)]J Fraisse, M F Bertheas, F Frère, et al.
Cytogenetics and Cell Genetics|January 1, 1980
Regional assignment of the ADA locus on 20q13.2 leads to qter by gene dosage studiesT Philip, G Lenoir, M O Rolland, et al.
Archives Francaises De Pediatrie|June 1, 1975
[Proceedings: Infantile cerebral poliodystrophy (Alper's disease) in an infant with hyperlactacidemia and hepatic pyruvate carboxylase]M David, P Baltassat, B Dinjon, et al.
Pageof 8

Showing results (61-70 of 79) with videos related to

Sort By:
Pageof 8
Pathologie-Biologie|October 14, 1998
[Interest of gene amplification by PCR for the diagnosis of Mycoplasma pneumoniae infections in the child]F Grattard, T Bourlet, C Galambrun, et al.
Journal De Genetique Humaine|March 1, 1981
[Early clinical and histopathological manifestations in 14 boys showing elevated serum creatine-phosphokinase levels in their first year]P Guibaud, H N Carrier, H Plauchu, et al.
Journal of Clinical Microbiology|March 1, 1994
Arbitrarily primed PCR, ribotyping, and plasmid pattern analysis applied to investigation of a nosocomial outbreak due to Enterobacter cloacae in a neonatal intensive care unitF Grattard, B Pozzetto, P Berthelot, et al.
Annales De Genetique|January 1, 1981
[Partial monosomy 20q: a new syndrome. Regional assignment of the adenosine deaminase (ADA) locus on 20q132 (author's transl)]J Fraisse, M F Bertheas, F Frère, et al.
Pediatrie|July 1, 1975
[Aseptic osteonecrosis following corticoid therapy and immunodepressive agents in children. Apropos of 3 observations]G Korkmaz, M David, B Parchoux, et al.
Journal De Genetique Humaine|March 1, 1979
[The present status of the chromosome map of man. I. Methods]T Philip, J Fraisse, P Guibaud, et al.
Gynecologie, Obstetrique & Fertilite|January 23, 2004
[A simple, low-cost and non-invasive method for screening Y microdeletions in infertile men]I Aknin-Seifer, R-L Touraine, H Lejeune, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|June 3, 1982
[Partial monosomy 20q : a new syndrome. Regional assignment of the ADA locus on 20q132 (author's transl)]J Fraisse, M F Bertheas, F Frère, et al.
Cytogenetics and Cell Genetics|January 1, 1980
Regional assignment of the ADA locus on 20q13.2 leads to qter by gene dosage studiesT Philip, G Lenoir, M O Rolland, et al.
Archives Francaises De Pediatrie|June 1, 1975
[Proceedings: Infantile cerebral poliodystrophy (Alper's disease) in an infant with hyperlactacidemia and hepatic pyruvate carboxylase]M David, P Baltassat, B Dinjon, et al.
Pageof 8