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A Munnich

Showing results (31-40 of 573) with videos related to

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Annales De Pediatrie|December 1, 1991
[Molecular genetics and prenatal diagnosis. Status and perspectives]A Munnich, S Lyonnet, J Kaplan, et al.
Annales D'Endocrinologie|January 1, 1996
[Association of achondroplasia to a mutation in the transmembrane domain of fibroblastic growth factor receptor 3 (FGFR3)]F Rousseau, J Bonaventure, M Le Merrer, et al.
Archives Francaises De Pediatrie|January 1, 1983
[Phenylalanine-restricted diet: the substitutes]H Ogier, E Depondt, A Munnich, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Genetic complementation analysis of mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency in cultured fibroblastsO Søvik, J M Saudubray, A Munnich, et al.
Archives Francaises De Pediatrie|January 1, 1983
[Phenylalanine-restricted diet. The portion-by-weight system]E Depondt, H Ogier, A Munnich, et al.
Pediatrie|January 1, 1992
[Molecular genetics and prenatal diagnosis]S Lyonnet, J M Rozet, C Martin, et al.
Journal of Medical Genetics|April 7, 2006
High incidence of SHOX anomalies in individuals with short statureC Huber, M Rosilio, A Munnich, et al.
Prenatal Diagnosis|June 1, 1992
Prenatal diagnosis of cytochrome c oxidase deficiency in cultured amniocytes is hazardousT Bourgeron, D Chrétien, A Rötig, et al.
Human Molecular Genetics|August 1, 1995
Spectrum of mitochondrial DNA rearrangements in the Pearson marrow-pancreas syndromeA Rötig, T Bourgeron, D Chretien, et al.
Archives Francaises De Pediatrie|October 1, 1987
[Prenatal screening for phenylketonuria in 2 families by trophoblast biopsy]F Rey, M Berthelon, A Munnich, et al.
Pageof 58

Showing results (31-40 of 573) with videos related to

Sort By:
Pageof 58
Annales De Pediatrie|December 1, 1991
[Molecular genetics and prenatal diagnosis. Status and perspectives]A Munnich, S Lyonnet, J Kaplan, et al.
Annales D'Endocrinologie|January 1, 1996
[Association of achondroplasia to a mutation in the transmembrane domain of fibroblastic growth factor receptor 3 (FGFR3)]F Rousseau, J Bonaventure, M Le Merrer, et al.
Archives Francaises De Pediatrie|January 1, 1983
[Phenylalanine-restricted diet: the substitutes]H Ogier, E Depondt, A Munnich, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Genetic complementation analysis of mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency in cultured fibroblastsO Søvik, J M Saudubray, A Munnich, et al.
Archives Francaises De Pediatrie|January 1, 1983
[Phenylalanine-restricted diet. The portion-by-weight system]E Depondt, H Ogier, A Munnich, et al.
Pediatrie|January 1, 1992
[Molecular genetics and prenatal diagnosis]S Lyonnet, J M Rozet, C Martin, et al.
Journal of Medical Genetics|April 7, 2006
High incidence of SHOX anomalies in individuals with short statureC Huber, M Rosilio, A Munnich, et al.
Prenatal Diagnosis|June 1, 1992
Prenatal diagnosis of cytochrome c oxidase deficiency in cultured amniocytes is hazardousT Bourgeron, D Chrétien, A Rötig, et al.
Human Molecular Genetics|August 1, 1995
Spectrum of mitochondrial DNA rearrangements in the Pearson marrow-pancreas syndromeA Rötig, T Bourgeron, D Chretien, et al.
Archives Francaises De Pediatrie|October 1, 1987
[Prenatal screening for phenylketonuria in 2 families by trophoblast biopsy]F Rey, M Berthelon, A Munnich, et al.
Pageof 58