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Investigative Ophthalmology & Visual Science
|
May 1, 1984
Aniridia: enzyme studies in an 11p--chromosomal deletion
J B Bateman, M C Sparkes, R S Sparkes
Science (New York, N.Y.)
|
September 8, 1978
Bone marrow origin of hepatic macrophages (Kupffer cells) in humans
R P Gale, R S Sparkes, D W Golde
American Journal of Medical Genetics
|
January 1, 1980
C-band polymorphism: comparison between trisomy 21 cases and mentally retarded controls
S J Funderburk, I Klisak, R S Sparkes, et al.
Journal of Medical Genetics
|
December 1, 1980
Craniosynostosis and syndactyly: expanding the 11q-- chromosomal deletion phenotype
B M Lippe, R S Sparkes, B Fass, et al.
Kroc Foundation Series
|
January 1, 1985
Genetic linkage studies in ataxia-telangiectasia: Gm markers
R A Gatti, M Boehnke, M Crist, et al.
American Journal of Hematology
|
May 1, 1993
Ph1-chromosome positive acute lymphoblastic leukemia: is t(9;22) the initial abnormality?
I Aurer, R S Sparkes, G Schiller, et al.
American Journal of Human Genetics
|
September 1, 1984
The steroid sulfatase locus on structurally abnormal inactive X chromosomes is expressed
L Immken, T Mohandas, R S Sparkes, et al.
Blood
|
December 1, 1981
Somatic cell hybrid analyses of hematopoietic differentiation
H P Koeffler, R S Sparkes, R Billing, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1981
Regional assignment of genes for human alpha-globin and phosphoglycollate phosphatase to the short arm of chromosome 16
H P Koeffler, R S Sparkes, H Stang, et al.
Journal of Pediatric Ophthalmology and Strabismus
|
July 1, 1986
Congenital ocular fibrosis syndrome associated with the Prader-Willi syndrome
B Kalpakian, J B Bateman, R S Sparkes, et al.
Page
of 28
Search research articles
Search
Showing results (51-60 of 272) with videos related to
Sort By:
Page
of 28
Investigative Ophthalmology & Visual Science
|
May 1, 1984
Aniridia: enzyme studies in an 11p--chromosomal deletion
J B Bateman, M C Sparkes, R S Sparkes
Science (New York, N.Y.)
|
September 8, 1978
Bone marrow origin of hepatic macrophages (Kupffer cells) in humans
R P Gale, R S Sparkes, D W Golde
American Journal of Medical Genetics
|
January 1, 1980
C-band polymorphism: comparison between trisomy 21 cases and mentally retarded controls
S J Funderburk, I Klisak, R S Sparkes, et al.
Journal of Medical Genetics
|
December 1, 1980
Craniosynostosis and syndactyly: expanding the 11q-- chromosomal deletion phenotype
B M Lippe, R S Sparkes, B Fass, et al.
Kroc Foundation Series
|
January 1, 1985
Genetic linkage studies in ataxia-telangiectasia: Gm markers
R A Gatti, M Boehnke, M Crist, et al.
American Journal of Hematology
|
May 1, 1993
Ph1-chromosome positive acute lymphoblastic leukemia: is t(9;22) the initial abnormality?
I Aurer, R S Sparkes, G Schiller, et al.
American Journal of Human Genetics
|
September 1, 1984
The steroid sulfatase locus on structurally abnormal inactive X chromosomes is expressed
L Immken, T Mohandas, R S Sparkes, et al.
Blood
|
December 1, 1981
Somatic cell hybrid analyses of hematopoietic differentiation
H P Koeffler, R S Sparkes, R Billing, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1981
Regional assignment of genes for human alpha-globin and phosphoglycollate phosphatase to the short arm of chromosome 16
H P Koeffler, R S Sparkes, H Stang, et al.
Journal of Pediatric Ophthalmology and Strabismus
|
July 1, 1986
Congenital ocular fibrosis syndrome associated with the Prader-Willi syndrome
B Kalpakian, J B Bateman, R S Sparkes, et al.
Page
of 28