Search research articles
Contact Us
Filters
Showing results (31-40 of 45) with videos related to
Page
of 5
Sort By:
Molecular and Cellular Biology
|
July 1, 1994
An in vivo assay for the reverse transcriptase of human retrotransposon L1 in Saccharomyces cerevisiae
B A Dombroski, Q Feng, S L Mathias, et al.
Blood
|
December 1, 1979
A molecular basis for hemoglobin-H disease in American blacks
J 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 diagnosis
S 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 evolution
A 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 site
S E Antonarakis, S H Irkin, T C Cheng, et al.
Genetics
|
June 21, 2005
Haplotype diversity in 11 candidate genes across four populations
T 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 disease
J 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 sequence
A 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 2
E 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 clefts
J W Park, J Cai, I McIntosh, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 45) with videos related to
Sort By:
Page
of 5
Molecular and Cellular Biology
|
July 1, 1994
An in vivo assay for the reverse transcriptase of human retrotransposon L1 in Saccharomyces cerevisiae
B A Dombroski, Q Feng, S L Mathias, et al.
Blood
|
December 1, 1979
A molecular basis for hemoglobin-H disease in American blacks
J 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 diagnosis
S 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 evolution
A 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 site
S E Antonarakis, S H Irkin, T C Cheng, et al.
Genetics
|
June 21, 2005
Haplotype diversity in 11 candidate genes across four populations
T 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 disease
J 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 sequence
A 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 2
E 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 clefts
J W Park, J Cai, I McIntosh, et al.
Page
of 5