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J FREZAL

Showing results (51-60 of 61) with videos related to

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Lancet (London, England)|August 13, 1983
Deficient liver biotinidase activity in multiple carboxylase deficiencyM Gaudry, A Munnich, J M Saudubray, et al.
Annales De Medecine Interne|January 1, 1986
[Palmoplantar keratosis associated with keratitis: hereditary hypertyrosinemia treated by diet]H Ogier, F Hervé, J M Saudubray, et al.
Ophtalmologie : Organe De La Societe Francaise D'Ophtalmologie|May 1, 1990
[Prenatal diagnosis of various hereditary blinding diseases]A Michel-Awad, J Kaplan, M L Briard, et al.
Annales De Genetique|January 1, 1985
Assignment to chromosome 12 of the gene coding for the human cell surface antigen CD9(p24) using the monoclonal antibody ALB6C Boucheix, Nguyen-van-Cong, J Y Perrot, et al.
Pediatric Research|March 1, 1982
Enzyme replacement therapy by transplantation of HLA-compatible fibroblasts in Sanfilippo syndrome: another trialA Munnich, J M Saudubray, M C Hors-Cayla, et al.
Annales De Pediatrie|February 1, 1986
["Hepatitis" indicative of congenital ornithine carbamoyltransferase deficiency]J Ramos Alves, J Pinto Ribeiro, J Magalhaes, et al.
Acta Paediatrica Scandinavica|January 1, 1982
Congenital lactic acidosis, alpha-ketoglutaric aciduria and variant form of maple syrup urine disease due to a single enzyme defect: dihydrolipoyl dehydrogenase deficiencyA Munnich, J M Saudubray, J Taylor, et al.
Annales De Genetique|January 1, 1989
The anonymous PAS45 probe detects RFLPs in 13q31M S Gross, A Sefiani, M F de Tand, et al.
Annales De Genetique|January 1, 1986
Panel of twenty-five independent man-rodent hybrids for human genetic marker mappingNguyen Van Cong, D Weil, C Finaz, et al.
Annals of Human Genetics|May 1, 1997
Report on the Fifth International Workshop on Chromosome 9 held at Eynsham, Oxfordshire, UK, September 4-6, 1996S Povey, J Attwood, B Chadwick, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Lancet (London, England)|August 13, 1983
Deficient liver biotinidase activity in multiple carboxylase deficiencyM Gaudry, A Munnich, J M Saudubray, et al.
Annales De Medecine Interne|January 1, 1986
[Palmoplantar keratosis associated with keratitis: hereditary hypertyrosinemia treated by diet]H Ogier, F Hervé, J M Saudubray, et al.
Ophtalmologie : Organe De La Societe Francaise D'Ophtalmologie|May 1, 1990
[Prenatal diagnosis of various hereditary blinding diseases]A Michel-Awad, J Kaplan, M L Briard, et al.
Annales De Genetique|January 1, 1985
Assignment to chromosome 12 of the gene coding for the human cell surface antigen CD9(p24) using the monoclonal antibody ALB6C Boucheix, Nguyen-van-Cong, J Y Perrot, et al.
Pediatric Research|March 1, 1982
Enzyme replacement therapy by transplantation of HLA-compatible fibroblasts in Sanfilippo syndrome: another trialA Munnich, J M Saudubray, M C Hors-Cayla, et al.
Annales De Pediatrie|February 1, 1986
["Hepatitis" indicative of congenital ornithine carbamoyltransferase deficiency]J Ramos Alves, J Pinto Ribeiro, J Magalhaes, et al.
Acta Paediatrica Scandinavica|January 1, 1982
Congenital lactic acidosis, alpha-ketoglutaric aciduria and variant form of maple syrup urine disease due to a single enzyme defect: dihydrolipoyl dehydrogenase deficiencyA Munnich, J M Saudubray, J Taylor, et al.
Annales De Genetique|January 1, 1989
The anonymous PAS45 probe detects RFLPs in 13q31M S Gross, A Sefiani, M F de Tand, et al.
Annales De Genetique|January 1, 1986
Panel of twenty-five independent man-rodent hybrids for human genetic marker mappingNguyen Van Cong, D Weil, C Finaz, et al.
Annals of Human Genetics|May 1, 1997
Report on the Fifth International Workshop on Chromosome 9 held at Eynsham, Oxfordshire, UK, September 4-6, 1996S Povey, J Attwood, B Chadwick, et al.
Pageof 7