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J L Mandel

Showing results (71-80 of 257) with videos related to

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Human Genetics|February 1, 1986
A case of female hemophilia with a 46,XXr karyotype studied with X-chromosome DNA probesS Gilgenkrantz, M E Briquel, J L Mandel, et al.
Cytogenetics and Cell Genetics|January 1, 1987
Report of the committee on the genetic constitution of the X and Y chromosomesK E Davies, J L Mandel, J Weissenbach, 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.
Biochemical and Biophysical Research Communications|March 27, 1970
Calf thymus RNA polymerases exhibit template specificityM Gniazdowski, J L Mandel, F Gissinger, et al.
Advances in Experimental Medicine and Biology|June 14, 2001
Pathological mechanisms in polyglutamine expansion diseasesD Devys, G Yvert, A Lunkes, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 5, 2001
A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2PA Schenck, B Bardoni, A Moro, et al.
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.
Pageof 26

Showing results (71-80 of 257) with videos related to

Sort By:
Pageof 26
Human Genetics|February 1, 1986
A case of female hemophilia with a 46,XXr karyotype studied with X-chromosome DNA probesS Gilgenkrantz, M E Briquel, J L Mandel, et al.
Cytogenetics and Cell Genetics|January 1, 1987
Report of the committee on the genetic constitution of the X and Y chromosomesK E Davies, J L Mandel, J Weissenbach, 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.
Biochemical and Biophysical Research Communications|March 27, 1970
Calf thymus RNA polymerases exhibit template specificityM Gniazdowski, J L Mandel, F Gissinger, et al.
Advances in Experimental Medicine and Biology|June 14, 2001
Pathological mechanisms in polyglutamine expansion diseasesD Devys, G Yvert, A Lunkes, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 5, 2001
A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2PA Schenck, B Bardoni, A Moro, et al.
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.
Pageof 26