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A F Scott

Showing results (31-40 of 45) with videos related to

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Molecular and Cellular Biology|July 1, 1994
An in vivo assay for the reverse transcriptase of human retrotransposon L1 in Saccharomyces cerevisiaeB A Dombroski, Q Feng, S L Mathias, et al.
Blood|December 1, 1979
A molecular basis for hemoglobin-H disease in American blacksJ A Phillips, A F Scott, K D Smith, et al.
American Journal of Human Genetics|January 1, 1981
Population heterogeneity of the Hpa I restriction site associated with the beta globin gene: implications for prenatal diagnosisS R Panny, A F Scott, K D Smith, et al.
Molecular Biology and Evolution|September 1, 1984
The sequence of the gorilla fetal globin genes: evidence for multiple gene conversions in human evolutionA F Scott, P Heath, S Trusko, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1984
beta-Thalassemia in American Blacks: novel mutations in the "TATA" box and an acceptor splice siteS E Antonarakis, S H Irkin, T C Cheng, et al.
Genetics|June 21, 2005
Haplotype diversity in 11 candidate genes across four populationsT H Beaty, M D Fallin, J B Hetmanski, et al.
Blood|June 1, 1980
Unequal crossing-over: a common basis of single alpha-globin genes in Asians and American blacks with hemoglobin-H diseaseJ A Phillips, T A Vik, A F Scott, et al.
Genomics|October 1, 1987
Origin of the human L1 elements: proposed progenitor genes deduced from a consensus DNA sequenceA F Scott, B J Schmeckpeper, M Abdelrazik, et al.
Nature Genetics|November 1, 1994
Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2E W Jabs, X Li, A F Scott, et al.
Journal of Medical Genetics|January 18, 2006
High throughput SNP and expression analyses of candidate genes for non-syndromic oral cleftsJ W Park, J Cai, I McIntosh, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
Molecular and Cellular Biology|July 1, 1994
An in vivo assay for the reverse transcriptase of human retrotransposon L1 in Saccharomyces cerevisiaeB A Dombroski, Q Feng, S L Mathias, et al.
Blood|December 1, 1979
A molecular basis for hemoglobin-H disease in American blacksJ A Phillips, A F Scott, K D Smith, et al.
American Journal of Human Genetics|January 1, 1981
Population heterogeneity of the Hpa I restriction site associated with the beta globin gene: implications for prenatal diagnosisS R Panny, A F Scott, K D Smith, et al.
Molecular Biology and Evolution|September 1, 1984
The sequence of the gorilla fetal globin genes: evidence for multiple gene conversions in human evolutionA F Scott, P Heath, S Trusko, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1984
beta-Thalassemia in American Blacks: novel mutations in the "TATA" box and an acceptor splice siteS E Antonarakis, S H Irkin, T C Cheng, et al.
Genetics|June 21, 2005
Haplotype diversity in 11 candidate genes across four populationsT H Beaty, M D Fallin, J B Hetmanski, et al.
Blood|June 1, 1980
Unequal crossing-over: a common basis of single alpha-globin genes in Asians and American blacks with hemoglobin-H diseaseJ A Phillips, T A Vik, A F Scott, et al.
Genomics|October 1, 1987
Origin of the human L1 elements: proposed progenitor genes deduced from a consensus DNA sequenceA F Scott, B J Schmeckpeper, M Abdelrazik, et al.
Nature Genetics|November 1, 1994
Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2E W Jabs, X Li, A F Scott, et al.
Journal of Medical Genetics|January 18, 2006
High throughput SNP and expression analyses of candidate genes for non-syndromic oral cleftsJ W Park, J Cai, I McIntosh, et al.
Pageof 5