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J L Mandel

Showing results (81-90 of 257) with videos related to

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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.
Human Molecular Genetics|November 1, 1992
Two hot spots of recombination in the DMD gene correlate with the deletion prone regionsC Oudet, A Hanauer, P Clemens, et al.
Cytogenetics and Cell Genetics|July 15, 2000
Assignment of NUFIP1 (nuclear FMRP interacting protein 1) gene to chromosome 13q14 and assignment of a pseudogene to chromosome 6q12B Bardoni, S Giglio, A Schenck, et al.
Nucleic Acids Research|July 24, 1987
A PstI RFLP detected by probe cpX73 (DXS159) in Xq11-q12B Arveiler, M H Hofker, A A Bergen, et al.
Genomics|August 1, 1991
Physical mapping of two loci (D9S5 and D9S15) tightly linked to Friedreich ataxia locus (FRDA) and identification of nearby CpG islands by pulse-field gel electrophoresisR Fujita, A Hanauer, A Vincent, et al.
American Journal of Medical Genetics|April 1, 1992
On some technical aspects of direct DNA diagnosis of the fragile X syndromeF Rousseau, D Heitz, V Biancalana, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1985
The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequencyI Oberlé, D Drayna, G Camerino, et al.
Pageof 26

Showing results (81-90 of 257) with videos related to

Sort By:
Pageof 26
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.
Human Molecular Genetics|November 1, 1992
Two hot spots of recombination in the DMD gene correlate with the deletion prone regionsC Oudet, A Hanauer, P Clemens, et al.
Cytogenetics and Cell Genetics|July 15, 2000
Assignment of NUFIP1 (nuclear FMRP interacting protein 1) gene to chromosome 13q14 and assignment of a pseudogene to chromosome 6q12B Bardoni, S Giglio, A Schenck, et al.
Nucleic Acids Research|July 24, 1987
A PstI RFLP detected by probe cpX73 (DXS159) in Xq11-q12B Arveiler, M H Hofker, A A Bergen, et al.
Genomics|August 1, 1991
Physical mapping of two loci (D9S5 and D9S15) tightly linked to Friedreich ataxia locus (FRDA) and identification of nearby CpG islands by pulse-field gel electrophoresisR Fujita, A Hanauer, A Vincent, et al.
American Journal of Medical Genetics|April 1, 1992
On some technical aspects of direct DNA diagnosis of the fragile X syndromeF Rousseau, D Heitz, V Biancalana, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1985
The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequencyI Oberlé, D Drayna, G Camerino, et al.
Pageof 26