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F S Collins

Showing results (121-130 of 297) with videos related to

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Genes, Chromosomes & Cancer|May 1, 1994
Loss of neurofibromin in adrenal gland tumors from patients with neurofibromatosis type ID H Gutmann, J L Cole, W J Stone, et al.
Science (New York, N.Y.)|October 20, 1995
Genetic discrimination and health insurance: an urgent need for reformK L Hudson, K H Rothenberg, L B Andrews, et al.
Nature Genetics|December 1, 1996
Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two-colour fluorescence analysisJ G Hacia, L C Brody, M S Chee, et al.
Human Genetics|January 1, 1994
Nonsense mutations at Arg-1947 in two cases of familial neurofibromatosis type 1 in JapaneseT Horiuchi, N Hatta, M Matsumoto, et al.
Human Mutation|January 1, 1996
Novel missense mutation (G314R) in a cystic fibrosis patient with hepatic failureS Z Nasr, T V Strong, M K Mansoura, et al.
Nucleic Acids Research|August 1, 1998
Two color hybridization analysis using high density oligonucleotide arrays and energy transfer dyesJ G Hacia, K Edgemon, B Sun, et al.
American Journal of Medical Genetics|August 14, 1995
17q inversion involving the neurofibromatosis type one locus in a family with neurofibromatosis type oneA Asamoah, K North, S Doran, et al.
Genomics|March 1, 1990
Localization of a human T-cell-specific gene, RANTES (D17S136E), to chromosome 17q11.2-q12T A Donlon, A M Krensky, M R Wallace, et al.
Nature|January 24, 1985
A point mutation in the A gamma-globin gene promoter in Greek hereditary persistence of fetal haemoglobinF S Collins, J E Metherall, M Yamakawa, et al.
Genomics|April 10, 1995
Identification of a new murine runt domain-containing gene, Cbfa3, and localization of the human homolog, CBFA3, to chromosome 1p35-pterC Wijmenga, N A Speck, N C Dracopoli, et al.
Pageof 30

Showing results (121-130 of 297) with videos related to

Sort By:
Pageof 30
Genes, Chromosomes & Cancer|May 1, 1994
Loss of neurofibromin in adrenal gland tumors from patients with neurofibromatosis type ID H Gutmann, J L Cole, W J Stone, et al.
Science (New York, N.Y.)|October 20, 1995
Genetic discrimination and health insurance: an urgent need for reformK L Hudson, K H Rothenberg, L B Andrews, et al.
Nature Genetics|December 1, 1996
Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two-colour fluorescence analysisJ G Hacia, L C Brody, M S Chee, et al.
Human Genetics|January 1, 1994
Nonsense mutations at Arg-1947 in two cases of familial neurofibromatosis type 1 in JapaneseT Horiuchi, N Hatta, M Matsumoto, et al.
Human Mutation|January 1, 1996
Novel missense mutation (G314R) in a cystic fibrosis patient with hepatic failureS Z Nasr, T V Strong, M K Mansoura, et al.
Nucleic Acids Research|August 1, 1998
Two color hybridization analysis using high density oligonucleotide arrays and energy transfer dyesJ G Hacia, K Edgemon, B Sun, et al.
American Journal of Medical Genetics|August 14, 1995
17q inversion involving the neurofibromatosis type one locus in a family with neurofibromatosis type oneA Asamoah, K North, S Doran, et al.
Genomics|March 1, 1990
Localization of a human T-cell-specific gene, RANTES (D17S136E), to chromosome 17q11.2-q12T A Donlon, A M Krensky, M R Wallace, et al.
Nature|January 24, 1985
A point mutation in the A gamma-globin gene promoter in Greek hereditary persistence of fetal haemoglobinF S Collins, J E Metherall, M Yamakawa, et al.
Genomics|April 10, 1995
Identification of a new murine runt domain-containing gene, Cbfa3, and localization of the human homolog, CBFA3, to chromosome 1p35-pterC Wijmenga, N A Speck, N C Dracopoli, et al.
Pageof 30