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F S Collins

Showing results (91-100 of 297) with videos related to

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Human Mutation|January 1, 1993
An African-American cystic fibrosis patient homozygous for a novel frameshift mutation associated with reduced CFTR mRNA levelsL S Smit, S Z Nasr, M C Iannuzzi, et al.
Genomics|June 1, 1990
Human chromosome 17 NotI linking clones and their use in long-range restriction mapping of the Miller-Dieker chromosome region (MDCR) in 17p13.3S A Ledbetter, M R Wallace, F S Collins, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1997
Cloning of the human NADH: ubiquinone oxidoreductase subunit B13: localization to chromosome 7q32 and identification of a pseudogene on 11p15M W Russell, S du Manoir, F S Collins, et al.
Nucleic Acids Research|February 25, 1989
Direct construction of a chromosome-specific NotI linking library from flow-sorted chromosomesM R Wallace, J W Fountain, A M Brereton, et al.
Genes, Chromosomes & Cancer|April 1, 1993
The human NME2 gene lies within 18kb of NME1 in chromosome 17S C Chandrasekharappa, L A Gross, S E King, et al.
Pediatrics|October 1, 1987
Familial apple peel jejunal atresia: surgical, genetic, and radiographic aspectsJ H Seashore, F S Collins, R I Markowitz, et al.
American Journal of Human Genetics|January 1, 1989
The von Recklinghausen neurofibromatosis region on chromosome 17--genetic and physical maps come into focusF S Collins, B A Ponder, B R Seizinger, et al.
Science (New York, N.Y.)|October 4, 1991
A bacterial system for investigating transport effects of cystic fibrosis--associated mutationsA L Gibson, L M Wagner, F S Collins, et al.
The Journal of Pediatrics|March 1, 1980
Neonatal argininosuccinic aciduria-survival after early diagnosis and dietary managementF S Collins, G K Summer, R P Schwartz, et al.
Human Molecular Genetics|June 1, 1993
A simple non-radioactive method for diagnosis of Huntington's diseaseJ M Valdes, D A Tagle, L W Elmer, et al.
Pageof 30

Showing results (91-100 of 297) with videos related to

Sort By:
Pageof 30
Human Mutation|January 1, 1993
An African-American cystic fibrosis patient homozygous for a novel frameshift mutation associated with reduced CFTR mRNA levelsL S Smit, S Z Nasr, M C Iannuzzi, et al.
Genomics|June 1, 1990
Human chromosome 17 NotI linking clones and their use in long-range restriction mapping of the Miller-Dieker chromosome region (MDCR) in 17p13.3S A Ledbetter, M R Wallace, F S Collins, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1997
Cloning of the human NADH: ubiquinone oxidoreductase subunit B13: localization to chromosome 7q32 and identification of a pseudogene on 11p15M W Russell, S du Manoir, F S Collins, et al.
Nucleic Acids Research|February 25, 1989
Direct construction of a chromosome-specific NotI linking library from flow-sorted chromosomesM R Wallace, J W Fountain, A M Brereton, et al.
Genes, Chromosomes & Cancer|April 1, 1993
The human NME2 gene lies within 18kb of NME1 in chromosome 17S C Chandrasekharappa, L A Gross, S E King, et al.
Pediatrics|October 1, 1987
Familial apple peel jejunal atresia: surgical, genetic, and radiographic aspectsJ H Seashore, F S Collins, R I Markowitz, et al.
American Journal of Human Genetics|January 1, 1989
The von Recklinghausen neurofibromatosis region on chromosome 17--genetic and physical maps come into focusF S Collins, B A Ponder, B R Seizinger, et al.
Science (New York, N.Y.)|October 4, 1991
A bacterial system for investigating transport effects of cystic fibrosis--associated mutationsA L Gibson, L M Wagner, F S Collins, et al.
The Journal of Pediatrics|March 1, 1980
Neonatal argininosuccinic aciduria-survival after early diagnosis and dietary managementF S Collins, G K Summer, R P Schwartz, et al.
Human Molecular Genetics|June 1, 1993
A simple non-radioactive method for diagnosis of Huntington's diseaseJ M Valdes, D A Tagle, L W Elmer, et al.
Pageof 30