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The Western Journal of Medicine
|
October 1, 1991
Molecular genetics of retinitis pigmentosa
D 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 translocation
L 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) syndrome
U 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 pedigree
H 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 disease
R E Champlin, S A Feig, R S Sparkes, et al.
Leukemia Research
|
January 1, 1991
Hybrid leukemia and the 5q-abnormality
G 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 correlation
S 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 syndrome
M 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.
Page
of 36
Search research articles
Search
Showing results (141-150 of 355) with videos related to
Sort By:
Page
of 36
The Western Journal of Medicine
|
October 1, 1991
Molecular genetics of retinitis pigmentosa
D 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 translocation
L 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) syndrome
U 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 pedigree
H 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 disease
R E Champlin, S A Feig, R S Sparkes, et al.
Leukemia Research
|
January 1, 1991
Hybrid leukemia and the 5q-abnormality
G 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 correlation
S 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 syndrome
M 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.
Page
of 36