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A Munnich

Showing results (161-170 of 573) with videos related to

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Human Molecular Genetics|October 9, 2001
Disabled early recruitment of antioxidant defenses in Friedreich's ataxiaK Chantrel-Groussard, V Geromel, H Puccio, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1995
[Gene localisation in 12q12 in Holt-Oram atrio-digital syndrome]D Bonnet, J Terrett, E Pequignot-Viegas, et al.
Journal of Medical Genetics|April 1, 1995
Exclusion of RET and Pax 3 loci in Waardenburg-Hirschsprung diseaseT Attié, M Till, A Pelet, et al.
European Journal of Pediatrics|April 1, 1993
3-Methylglutaconic aciduria in a patient with Pearson syndromeU Lichter-Konecki, F K Trefz, A Rötig, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 17, 1999
[Contribution of genetics]S Lyonnet, N Morichon, M Dommergues, et al.
Prenatal Diagnosis|April 5, 2001
Denaturing high-performance liquid chromatography (DHPLC)-based prenatal diagnosis for tuberous sclerosisP Bénit, J P Bonnefont, A Kara Mostefa, et al.
American Journal of Medical Genetics|August 15, 1994
Apparent genetic homogeneity of the Treacher Collins-Franceschetti syndromeP Edery, Y Manach, M Le Merrer, et al.
Presse Medicale (Paris, France : 1983)|October 22, 1994
[Hypertrophic cardiomyopathy caused by cytochrome-oxidase deficiency]V Gournay-Toulemonde, A Munnich, J B Bouhour, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 1, 1997
[Beta mannosidosis: a new case]E Gourrier, M P Thomas, A Munnich, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 1, 1994
Biochemical and molecular investigations in respiratory chain deficienciesP Rustin, D Chretien, T Bourgeron, et al.
Pageof 58

Showing results (161-170 of 573) with videos related to

Sort By:
Pageof 58
Human Molecular Genetics|October 9, 2001
Disabled early recruitment of antioxidant defenses in Friedreich's ataxiaK Chantrel-Groussard, V Geromel, H Puccio, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1995
[Gene localisation in 12q12 in Holt-Oram atrio-digital syndrome]D Bonnet, J Terrett, E Pequignot-Viegas, et al.
Journal of Medical Genetics|April 1, 1995
Exclusion of RET and Pax 3 loci in Waardenburg-Hirschsprung diseaseT Attié, M Till, A Pelet, et al.
European Journal of Pediatrics|April 1, 1993
3-Methylglutaconic aciduria in a patient with Pearson syndromeU Lichter-Konecki, F K Trefz, A Rötig, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 17, 1999
[Contribution of genetics]S Lyonnet, N Morichon, M Dommergues, et al.
Prenatal Diagnosis|April 5, 2001
Denaturing high-performance liquid chromatography (DHPLC)-based prenatal diagnosis for tuberous sclerosisP Bénit, J P Bonnefont, A Kara Mostefa, et al.
American Journal of Medical Genetics|August 15, 1994
Apparent genetic homogeneity of the Treacher Collins-Franceschetti syndromeP Edery, Y Manach, M Le Merrer, et al.
Presse Medicale (Paris, France : 1983)|October 22, 1994
[Hypertrophic cardiomyopathy caused by cytochrome-oxidase deficiency]V Gournay-Toulemonde, A Munnich, J B Bouhour, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 1, 1997
[Beta mannosidosis: a new case]E Gourrier, M P Thomas, A Munnich, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 1, 1994
Biochemical and molecular investigations in respiratory chain deficienciesP Rustin, D Chretien, T Bourgeron, et al.
Pageof 58