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S Sparkes

Showing results (141-150 of 355) with videos related to

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The Western Journal of Medicine|October 1, 1991
Molecular genetics of retinitis pigmentosaD B Farber, J R Heckenlively, R S Sparkes, et al.
Science (New York, N.Y.)|September 25, 1981
Familial retinoblastoma and chromosome 13 deletion transmitted via an insertional translocationL C Strong, V M Riccardi, R E Ferrell, et al.
Birth Defects Original Article Series|January 1, 1977
Duplication 11 (q21 to 23 leads to qter) syndromeU Francke, F Weber, R S Sparkes, et al.
Journal of Medical Genetics|December 1, 1970
Cytogenetic studies in a patient with a de novo t(Cq-;Gp+)B F Crandall, R E Carrel, G L Adams, et al.
The Journal of Pediatrics|April 1, 1981
Congenital contractural arachnodactyly, keratoconus, and probable Marfan syndrome in the same pedigreeH N Bass, R S Sparkes, B F Crandall, et al.
British Journal of Haematology|March 1, 1984
Bone marrow transplantation from identical twins in the treatment of aplastic anaemia: implication for the pathogenesis of the diseaseR E Champlin, S A Feig, R S Sparkes, et al.
Leukemia Research|January 1, 1991
Hybrid leukemia and the 5q-abnormalityG Sun, S Wormsley, R S Sparkes, et al.
Human Genetics|January 1, 1979
Prominent acrocentric chromosome satellites in child patients with mental retardation or psychiatric disorders; no IQ-satellite size correlationS J Funderburk, I Goldenberg, I Klisak, et al.
Cancer Genetics and Cytogenetics|December 1, 1987
Trisomy 12 in Burkitt-like lymphoma associated with acquired immunodeficiency syndromeM A Kosmo, R T Mitsuyasu, R S Sparkes, et al.
American Journal of Medical Genetics|December 1, 1982
A 15 leads to 1 translocation in a patient mosaic for presence or absence of an isodic(15p)(q11)E A Wulfsberg, R S Sparkes, I J Klisak, et al.
Pageof 36

Showing results (141-150 of 355) with videos related to

Sort By:
Pageof 36
The Western Journal of Medicine|October 1, 1991
Molecular genetics of retinitis pigmentosaD B Farber, J R Heckenlively, R S Sparkes, et al.
Science (New York, N.Y.)|September 25, 1981
Familial retinoblastoma and chromosome 13 deletion transmitted via an insertional translocationL C Strong, V M Riccardi, R E Ferrell, et al.
Birth Defects Original Article Series|January 1, 1977
Duplication 11 (q21 to 23 leads to qter) syndromeU Francke, F Weber, R S Sparkes, et al.
Journal of Medical Genetics|December 1, 1970
Cytogenetic studies in a patient with a de novo t(Cq-;Gp+)B F Crandall, R E Carrel, G L Adams, et al.
The Journal of Pediatrics|April 1, 1981
Congenital contractural arachnodactyly, keratoconus, and probable Marfan syndrome in the same pedigreeH N Bass, R S Sparkes, B F Crandall, et al.
British Journal of Haematology|March 1, 1984
Bone marrow transplantation from identical twins in the treatment of aplastic anaemia: implication for the pathogenesis of the diseaseR E Champlin, S A Feig, R S Sparkes, et al.
Leukemia Research|January 1, 1991
Hybrid leukemia and the 5q-abnormalityG Sun, S Wormsley, R S Sparkes, et al.
Human Genetics|January 1, 1979
Prominent acrocentric chromosome satellites in child patients with mental retardation or psychiatric disorders; no IQ-satellite size correlationS J Funderburk, I Goldenberg, I Klisak, et al.
Cancer Genetics and Cytogenetics|December 1, 1987
Trisomy 12 in Burkitt-like lymphoma associated with acquired immunodeficiency syndromeM A Kosmo, R T Mitsuyasu, R S Sparkes, et al.
American Journal of Medical Genetics|December 1, 1982
A 15 leads to 1 translocation in a patient mosaic for presence or absence of an isodic(15p)(q11)E A Wulfsberg, R S Sparkes, I J Klisak, et al.
Pageof 36