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F S Collins

Showing results (111-120 of 297) with videos related to

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The American Journal of Surgical Pathology|July 1, 1984
Infantile myofibromatosis. Evidence for an autosomal-dominant disorderT A Jennings, P H Duray, F S Collins, et al.
Human Molecular Genetics|July 1, 1993
Dinucleotide repeat polymorphisms at the D4S126 and D4S114 lociD A Tagle, K L Blanchard-McQuate, J Valdes, et al.
Human Molecular Genetics|July 1, 1993
A compound nucleotide repeat in the neurofibromatosis (NF1) geneL B Andersen, S A Tarlé, D A Marchuk, et al.
Human Molecular Genetics|May 1, 1994
Ten base pair duplication in exon 38 of the NF1 geneE Legius, B K Hall, M R Wallace, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1984
G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma geneF S Collins, C J Stoeckert, G R Serjeant, et al.
Somatic Cell and Molecular Genetics|September 1, 1996
Chromosomal localization of 15 ion channel genesM W Russell, S du Manoir, D J Munroe, et al.
Progress in Clinical and Biological Research|January 1, 1989
Nuclear proteins which bind the human gamma-globin geneD L Gumucio, T A Gray, K L Rood, et al.
Nucleic Acids Research|August 25, 1987
SacI RFLP in the human von Willebrand factor geneB A Konkle, S Kim, M C Iannuzzi, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1993
Functional roles of the nucleotide-binding folds in the activation of the cystic fibrosis transmembrane conductance regulatorL S Smit, D J Wilkinson, M K Mansoura, et al.
Journal of Neuroscience Research|October 1, 1993
Modulation of the neurofibromatosis type 1 gene product, neurofibromin, during Schwann cell differentiationD H Gutmann, G I Tennekoon, J L Cole, et al.
Pageof 30

Showing results (111-120 of 297) with videos related to

Sort By:
Pageof 30
The American Journal of Surgical Pathology|July 1, 1984
Infantile myofibromatosis. Evidence for an autosomal-dominant disorderT A Jennings, P H Duray, F S Collins, et al.
Human Molecular Genetics|July 1, 1993
Dinucleotide repeat polymorphisms at the D4S126 and D4S114 lociD A Tagle, K L Blanchard-McQuate, J Valdes, et al.
Human Molecular Genetics|July 1, 1993
A compound nucleotide repeat in the neurofibromatosis (NF1) geneL B Andersen, S A Tarlé, D A Marchuk, et al.
Human Molecular Genetics|May 1, 1994
Ten base pair duplication in exon 38 of the NF1 geneE Legius, B K Hall, M R Wallace, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1984
G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma geneF S Collins, C J Stoeckert, G R Serjeant, et al.
Somatic Cell and Molecular Genetics|September 1, 1996
Chromosomal localization of 15 ion channel genesM W Russell, S du Manoir, D J Munroe, et al.
Progress in Clinical and Biological Research|January 1, 1989
Nuclear proteins which bind the human gamma-globin geneD L Gumucio, T A Gray, K L Rood, et al.
Nucleic Acids Research|August 25, 1987
SacI RFLP in the human von Willebrand factor geneB A Konkle, S Kim, M C Iannuzzi, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1993
Functional roles of the nucleotide-binding folds in the activation of the cystic fibrosis transmembrane conductance regulatorL S Smit, D J Wilkinson, M K Mansoura, et al.
Journal of Neuroscience Research|October 1, 1993
Modulation of the neurofibromatosis type 1 gene product, neurofibromin, during Schwann cell differentiationD H Gutmann, G I Tennekoon, J L Cole, et al.
Pageof 30