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Blood
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January 1, 1988
The gene for protein S maps near the centromere of human chromosome 3
P C Watkins, R Eddy, Y Fukushima, et al.
Nucleic Acids Research
|
September 11, 1985
Isolation of polymorphic DNA segments from human chromosome 21
P C Watkins, R E Tanzi, K T Gibbons, et al.
Cytogenetics and Cell Genetics
|
January 1, 1986
Regional assignment of the erythropoietin gene to human chromosome region 7pter----q22
P C Watkins, R Eddy, N Hoffman, et al.
The New England Journal of Medicine
|
October 11, 1990
Linkage of dominant hereditary spherocytosis to the gene for the erythrocyte membrane-skeleton protein ankyrin
F F Costa, P Agre, P C Watkins, et al.
American Journal of Human Genetics
|
March 1, 1989
Genealogical analysis of cystic fibrosis families and chromosome 7q RFLP haplotypes in the Hutterite Brethren
T M Fujiwara, K Morgan, R H Schwartz, et al.
Annals of the New York Academy of Sciences
|
January 1, 1985
Genetic linkage map for chromosome 21
J F Gusella, R E Tanzi, P C Watkins, et al.
American Journal of Human Genetics
|
October 1, 1988
Molecular and cytogenetic characterization of a de novo t(5p;21q) in a patient previously diagnosed as monosomy 21
M C Phelan, C C Morton, R E Stevenson, et al.
Annals of the New York Academy of Sciences
|
January 1, 1985
Ring chromosome 21: characterization of DNA sequences at sites of breakage and reunion
H H Kazazian, S E Antonarakis, C Wong, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1989
Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome
Z Rahmani, J L Blouin, N Creau-Goldberg, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1990
Down syndrome critical region around D21S55 on proximal 21q22.3
Z Rahmani, J L Blouin, N Créau-Goldberg, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 53) with videos related to
Sort By:
Page
of 6
Blood
|
January 1, 1988
The gene for protein S maps near the centromere of human chromosome 3
P C Watkins, R Eddy, Y Fukushima, et al.
Nucleic Acids Research
|
September 11, 1985
Isolation of polymorphic DNA segments from human chromosome 21
P C Watkins, R E Tanzi, K T Gibbons, et al.
Cytogenetics and Cell Genetics
|
January 1, 1986
Regional assignment of the erythropoietin gene to human chromosome region 7pter----q22
P C Watkins, R Eddy, N Hoffman, et al.
The New England Journal of Medicine
|
October 11, 1990
Linkage of dominant hereditary spherocytosis to the gene for the erythrocyte membrane-skeleton protein ankyrin
F F Costa, P Agre, P C Watkins, et al.
American Journal of Human Genetics
|
March 1, 1989
Genealogical analysis of cystic fibrosis families and chromosome 7q RFLP haplotypes in the Hutterite Brethren
T M Fujiwara, K Morgan, R H Schwartz, et al.
Annals of the New York Academy of Sciences
|
January 1, 1985
Genetic linkage map for chromosome 21
J F Gusella, R E Tanzi, P C Watkins, et al.
American Journal of Human Genetics
|
October 1, 1988
Molecular and cytogenetic characterization of a de novo t(5p;21q) in a patient previously diagnosed as monosomy 21
M C Phelan, C C Morton, R E Stevenson, et al.
Annals of the New York Academy of Sciences
|
January 1, 1985
Ring chromosome 21: characterization of DNA sequences at sites of breakage and reunion
H H Kazazian, S E Antonarakis, C Wong, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1989
Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome
Z Rahmani, J L Blouin, N Creau-Goldberg, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1990
Down syndrome critical region around D21S55 on proximal 21q22.3
Z Rahmani, J L Blouin, N Créau-Goldberg, et al.
Page
of 6