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P Guibaud

Showing results (111-120 of 147) with videos related to

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Journal De Genetique Humaine|June 1, 1979
[The status of chromosome mapping in man. II. Results and applications]T Philip, J Fraisse, I Philip, et al.
Human Mutation|January 1, 1993
Hunter syndrome: gene deletions and rearrangementsR Froissart, J L Blond, I Maire, et al.
Pediatrie|April 1, 1977
[Severe, intractable, familial infantile diarrhea, without known cause]F Larbre, A Frédérich, P Guibaud, et al.
Journal De Genetique Humaine|March 1, 1981
[Neonatal screening for duchenne myopathy by serum elevation of creatine phosphokinase activity. 5 years experience]H Plauchu, C Dellamonica, B Pascal, et al.
Archives Francaises De Pediatrie|August 1, 1988
[Lethal syndromes with thin bones]P Maroteaux, L Cohen-Solal, J Bonaventure, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Early prenatal diagnosis of propionic acidaemia with simultaneous sampling of chorionic villus and amniotic fluidM O Rolland, P Divry, G Mandon, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|December 21, 2002
Surgery of chronic traumatic aneurysm of the aortic isthmus: benefit of direct sutureX Roques, J Remes, M N Laborde, et al.
Pediatrie|December 1, 1978
[Fabry's disease. Initial nephrogenic diabetes insipidus in children]B Parchoux, P Guibaud, I Maire, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Isolated 3-methylcrotonyl-CoA carboxylase deficiency in a 16-month-old childM O Rolland, P Divry, M T Zabot, et al.
Pediatrie|January 1, 1993
[Multiple acyl-CoA dehydrogenase deficiency. Report of 2 siblings]N Guffon, C Vianey-Saban, J C Berthier, et al.
Pageof 15

Showing results (111-120 of 147) with videos related to

Sort By:
Pageof 15
Journal De Genetique Humaine|June 1, 1979
[The status of chromosome mapping in man. II. Results and applications]T Philip, J Fraisse, I Philip, et al.
Human Mutation|January 1, 1993
Hunter syndrome: gene deletions and rearrangementsR Froissart, J L Blond, I Maire, et al.
Pediatrie|April 1, 1977
[Severe, intractable, familial infantile diarrhea, without known cause]F Larbre, A Frédérich, P Guibaud, et al.
Journal De Genetique Humaine|March 1, 1981
[Neonatal screening for duchenne myopathy by serum elevation of creatine phosphokinase activity. 5 years experience]H Plauchu, C Dellamonica, B Pascal, et al.
Archives Francaises De Pediatrie|August 1, 1988
[Lethal syndromes with thin bones]P Maroteaux, L Cohen-Solal, J Bonaventure, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Early prenatal diagnosis of propionic acidaemia with simultaneous sampling of chorionic villus and amniotic fluidM O Rolland, P Divry, G Mandon, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|December 21, 2002
Surgery of chronic traumatic aneurysm of the aortic isthmus: benefit of direct sutureX Roques, J Remes, M N Laborde, et al.
Pediatrie|December 1, 1978
[Fabry's disease. Initial nephrogenic diabetes insipidus in children]B Parchoux, P Guibaud, I Maire, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Isolated 3-methylcrotonyl-CoA carboxylase deficiency in a 16-month-old childM O Rolland, P Divry, M T Zabot, et al.
Pediatrie|January 1, 1993
[Multiple acyl-CoA dehydrogenase deficiency. Report of 2 siblings]N Guffon, C Vianey-Saban, J C Berthier, et al.
Pageof 15