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O Attree

Showing results (1-10 of 8) with videos related to

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Annales Pharmaceutiques Francaises|February 12, 2000
[Natural biological risks and military biological risks]P Michel, O Attree, R Mage, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Isolation of cDNA sequences around the chromosomal breakpoint in a female with Lowe syndrome by direct screening of cDNA libraries with yeast artificial chromosomesI Okabe, O Attree, L C Bailey, et al.
Genomics|April 1, 1989
Mutations in the catalytic domain of human coagulation factor IX: rapid characterization by direct genomic sequencing of DNA fragments displaying an altered melting behaviorO Attree, D Vidaud, M Vidaud, et al.
The New England Journal of Medicine|October 12, 1989
Laron dwarfism and mutations of the growth hormone-receptor geneS Amselem, P Duquesnoy, O Attree, et al.
Archives Francaises De Pediatrie|December 1, 1988
[Bronchiolitis caused by respiratory syncytial virus in very young infants and transmitted maternal antibodies]O Attree, F Tourangeau, G De Saint-Maur, et al.
Human Genetics|September 1, 1990
Frequency of the cystic fibrosis delta F508 mutation in a large sample of the French populationM Vidaud, C Ferec, O Attree, et al.
Nature|July 16, 1992
The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphataseO Attree, I M Olivos, I Okabe, et al.
Nucleic Acids Research|September 11, 1992
Cloning of human and bovine homologs of SNF2/SWI2: a global activator of transcription in yeast S. cerevisiaeI Okabe, L C Bailey, O Attree, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Annales Pharmaceutiques Francaises|February 12, 2000
[Natural biological risks and military biological risks]P Michel, O Attree, R Mage, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Isolation of cDNA sequences around the chromosomal breakpoint in a female with Lowe syndrome by direct screening of cDNA libraries with yeast artificial chromosomesI Okabe, O Attree, L C Bailey, et al.
Genomics|April 1, 1989
Mutations in the catalytic domain of human coagulation factor IX: rapid characterization by direct genomic sequencing of DNA fragments displaying an altered melting behaviorO Attree, D Vidaud, M Vidaud, et al.
The New England Journal of Medicine|October 12, 1989
Laron dwarfism and mutations of the growth hormone-receptor geneS Amselem, P Duquesnoy, O Attree, et al.
Archives Francaises De Pediatrie|December 1, 1988
[Bronchiolitis caused by respiratory syncytial virus in very young infants and transmitted maternal antibodies]O Attree, F Tourangeau, G De Saint-Maur, et al.
Human Genetics|September 1, 1990
Frequency of the cystic fibrosis delta F508 mutation in a large sample of the French populationM Vidaud, C Ferec, O Attree, et al.
Nature|July 16, 1992
The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphataseO Attree, I M Olivos, I Okabe, et al.
Nucleic Acids Research|September 11, 1992
Cloning of human and bovine homologs of SNF2/SWI2: a global activator of transcription in yeast S. cerevisiaeI Okabe, L C Bailey, O Attree, et al.
Pageof 1