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J L Mandel

Showing results (131-140 of 257) with videos related to

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Nucleic Acids Research|February 25, 1987
RFLPs for the human erythrocyte membrane glycophorin C geneB Arveiler, C Le Van Kim, Y Colin, et al.
American Journal of Human Genetics|January 1, 1990
The Friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15A Hanauer, M Chery, R Fujita, et al.
Human Molecular Genetics|September 26, 2000
Myotubularin, a phosphatase deficient in myotubular myopathy, acts on phosphatidylinositol 3-kinase and phosphatidylinositol 3-phosphate pathwayF Blondeau, J Laporte, S Bodin, et al.
Cytogenetics and Cell Genetics|January 1, 1988
Report of the committee on the genetic constitution of the X chromosomeJ L Mandel, H F Willard, R L Nussbaum, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Report and abstracts of the Fourth International Workshop on Human X Chromosome Mapping 1993. St. Louis, Missouri, May 9-12, 1993D Schlessinger, J L Mandel, A P Monaco, et al.
Human Molecular Genetics|October 1, 1994
Missense mutations are frequent in the gene for X-chromosomal adrenoleukodystrophy (ALD)S Fuchs, C O Sarde, H Wedemann, et al.
Revue Neurologique|August 14, 2013
Adult centronuclear myopathies: A hospital-based studyA Echaniz-Laguna, V Biancalana, J Böhm, et al.
Basic Life Sciences|January 1, 1974
Transcription of double-stranded viral and cellular DNAs by purified mammalian DNA-dependent RNA polymerasesP Chambon, J L Mandel, F Gissinger, et al.
Genomics|July 1, 1988
Isolation and characterization of a family of sequences dispersed on the human X chromosomeB Bardoni, S Guioli, E Raimondi, et al.
Genomics|November 1, 1989
The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locusA Vincent, N Dahl, I Oberlé, et al.
Pageof 26

Showing results (131-140 of 257) with videos related to

Sort By:
Pageof 26
Nucleic Acids Research|February 25, 1987
RFLPs for the human erythrocyte membrane glycophorin C geneB Arveiler, C Le Van Kim, Y Colin, et al.
American Journal of Human Genetics|January 1, 1990
The Friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15A Hanauer, M Chery, R Fujita, et al.
Human Molecular Genetics|September 26, 2000
Myotubularin, a phosphatase deficient in myotubular myopathy, acts on phosphatidylinositol 3-kinase and phosphatidylinositol 3-phosphate pathwayF Blondeau, J Laporte, S Bodin, et al.
Cytogenetics and Cell Genetics|January 1, 1988
Report of the committee on the genetic constitution of the X chromosomeJ L Mandel, H F Willard, R L Nussbaum, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Report and abstracts of the Fourth International Workshop on Human X Chromosome Mapping 1993. St. Louis, Missouri, May 9-12, 1993D Schlessinger, J L Mandel, A P Monaco, et al.
Human Molecular Genetics|October 1, 1994
Missense mutations are frequent in the gene for X-chromosomal adrenoleukodystrophy (ALD)S Fuchs, C O Sarde, H Wedemann, et al.
Revue Neurologique|August 14, 2013
Adult centronuclear myopathies: A hospital-based studyA Echaniz-Laguna, V Biancalana, J Böhm, et al.
Basic Life Sciences|January 1, 1974
Transcription of double-stranded viral and cellular DNAs by purified mammalian DNA-dependent RNA polymerasesP Chambon, J L Mandel, F Gissinger, et al.
Genomics|July 1, 1988
Isolation and characterization of a family of sequences dispersed on the human X chromosomeB Bardoni, S Guioli, E Raimondi, et al.
Genomics|November 1, 1989
The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locusA Vincent, N Dahl, I Oberlé, et al.
Pageof 26