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J Rey
F Rey

Showing results (41-50 of 820) with videos related to

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Journal of Medical Genetics|March 1, 1993
Genetic background of clinical homogeneity of phenylketonuria in PolandJ Jaruzelska, R Matuszak, S Lyonnet, et al.
Human Molecular Genetics|January 1, 1993
Illegitimate transcription of the phenylalanine hydroxylase gene in lymphocytes for identification of mutations in phenylketonuriaV Abadie, J Jaruzelska, S Lyonnet, et al.
Human Genetics|January 1, 1985
Maple syrup urine disease: two different forms within a single familyJ Frézal, O Amédée-Manesme, G Mitchell, et al.
European Journal of Pediatrics|January 1, 1987
Intellectual and school performances in early-treated classical PKU patients. The French collaborative studyJ M Saudubray, F Rey, H Ogier, et al.
Archives Francaises De Pediatrie|October 1, 1992
[Phenotypic expression of 12 mutations of the phenylalanine hydroxylase gene]F Rey, V Abadie, S Lyonnet, et al.
Genomics|November 1, 1989
CpG dinucleotides are mutation hot spots in phenylketonuriaV Abadie, S Lyonnet, N Maurin, et al.
The Journal of Biological Chemistry|May 25, 1991
A 3-base pair in-frame deletion of the phenylalanine hydroxylase gene results in a kinetic variant of phenylketonuriaC Caillaud, S Lyonnet, F Rey, et al.
Endoscopy|February 26, 2000
Protocol for reprocessing endoscopic accessories. European Society of Gastrointestinal EndoscopyJ F Rey
Annales De Chirurgie|January 1, 1993
[Is your scalpel correctly adjusted? The correct use of electric scalpels in digestive system endoscopy]J F Rey
Gastrointestinal Endoscopy|December 16, 1998
Overuse or underuse of endoscopy? The optimal indicationsJ F Rey
Pageof 82

Showing results (41-50 of 820) with videos related to

Sort By:
Pageof 82
Journal of Medical Genetics|March 1, 1993
Genetic background of clinical homogeneity of phenylketonuria in PolandJ Jaruzelska, R Matuszak, S Lyonnet, et al.
Human Molecular Genetics|January 1, 1993
Illegitimate transcription of the phenylalanine hydroxylase gene in lymphocytes for identification of mutations in phenylketonuriaV Abadie, J Jaruzelska, S Lyonnet, et al.
Human Genetics|January 1, 1985
Maple syrup urine disease: two different forms within a single familyJ Frézal, O Amédée-Manesme, G Mitchell, et al.
European Journal of Pediatrics|January 1, 1987
Intellectual and school performances in early-treated classical PKU patients. The French collaborative studyJ M Saudubray, F Rey, H Ogier, et al.
Archives Francaises De Pediatrie|October 1, 1992
[Phenotypic expression of 12 mutations of the phenylalanine hydroxylase gene]F Rey, V Abadie, S Lyonnet, et al.
Genomics|November 1, 1989
CpG dinucleotides are mutation hot spots in phenylketonuriaV Abadie, S Lyonnet, N Maurin, et al.
The Journal of Biological Chemistry|May 25, 1991
A 3-base pair in-frame deletion of the phenylalanine hydroxylase gene results in a kinetic variant of phenylketonuriaC Caillaud, S Lyonnet, F Rey, et al.
Endoscopy|February 26, 2000
Protocol for reprocessing endoscopic accessories. European Society of Gastrointestinal EndoscopyJ F Rey
Annales De Chirurgie|January 1, 1993
[Is your scalpel correctly adjusted? The correct use of electric scalpels in digestive system endoscopy]J F Rey
Gastrointestinal Endoscopy|December 16, 1998
Overuse or underuse of endoscopy? The optimal indicationsJ F Rey
Pageof 82