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L Mandel

Showing results (211-220 of 451) with videos related to

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Cell|July 1, 1980
The ovalbumin gene family: structure of the X gene and evolution of duplicated split genesR Heilig, F Perrin, F Gannon, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Mental retardation in fragile X syndrome]J L Mandel, V Biancalana, M Cossée, et al.
Revue D'Epidemiologie Et De Sante Publique|January 1, 1995
[Comparative analysis of the costs of cytogenetic techniques and molecular biology techniques in the diagnosis of fragile X disease]I Hirtzlin, J L Mandel, J L Lanoé, et al.
FEBS Letters|May 16, 1994
The protein coded by the X-adrenoleukodystrophy gene is a peroxisomal integral membrane proteinM Contreras, J Mosser, J L Mandel, et al.
European Journal of Biochemistry|July 13, 1972
Animal DNA-dependent RNA polymerases. 1. Large-scale solubilization and separation of A and B calf-thymus RNA-polymerase activitiesC Kedinger, F Gissinger, M Gniazdowski, et al.
Nucleic Acids Research|August 26, 1986
A new RFLP for D18S3(B74) an anonymous genomic clone localized to 18p113L Ozelius, J L Mandel, J F Gusella, et al.
Cell Biology International|April 1, 1994
Protective effects of Nocardia delipidated cell mitogen on the mucosa of the small intestine after irradiation of germ-free pigletsH Kozakova, L Mandel, I Trebichavsky, et al.
Journal of Medical Genetics|November 1, 1992
Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutationD Heitz, D Devys, G Imbert, et al.
Revue Neurologique|December 19, 2000
[Myotubular myopathy]C Guiraud-Chaumeil, J Laporte, J L Mandel, et al.
Human Molecular Genetics|June 1, 1994
The Friedreich ataxia region: characterization of two novel genes and reduction of the critical region to 300 kbF Duclos, F Rodius, K Wrogemann, et al.
Pageof 46

Showing results (211-220 of 451) with videos related to

Sort By:
Pageof 46
Cell|July 1, 1980
The ovalbumin gene family: structure of the X gene and evolution of duplicated split genesR Heilig, F Perrin, F Gannon, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Mental retardation in fragile X syndrome]J L Mandel, V Biancalana, M Cossée, et al.
Revue D'Epidemiologie Et De Sante Publique|January 1, 1995
[Comparative analysis of the costs of cytogenetic techniques and molecular biology techniques in the diagnosis of fragile X disease]I Hirtzlin, J L Mandel, J L Lanoé, et al.
FEBS Letters|May 16, 1994
The protein coded by the X-adrenoleukodystrophy gene is a peroxisomal integral membrane proteinM Contreras, J Mosser, J L Mandel, et al.
European Journal of Biochemistry|July 13, 1972
Animal DNA-dependent RNA polymerases. 1. Large-scale solubilization and separation of A and B calf-thymus RNA-polymerase activitiesC Kedinger, F Gissinger, M Gniazdowski, et al.
Nucleic Acids Research|August 26, 1986
A new RFLP for D18S3(B74) an anonymous genomic clone localized to 18p113L Ozelius, J L Mandel, J F Gusella, et al.
Cell Biology International|April 1, 1994
Protective effects of Nocardia delipidated cell mitogen on the mucosa of the small intestine after irradiation of germ-free pigletsH Kozakova, L Mandel, I Trebichavsky, et al.
Journal of Medical Genetics|November 1, 1992
Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutationD Heitz, D Devys, G Imbert, et al.
Revue Neurologique|December 19, 2000
[Myotubular myopathy]C Guiraud-Chaumeil, J Laporte, J L Mandel, et al.
Human Molecular Genetics|June 1, 1994
The Friedreich ataxia region: characterization of two novel genes and reduction of the critical region to 300 kbF Duclos, F Rodius, K Wrogemann, et al.
Pageof 46