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R B Surana

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American Journal of Diseases of Children (1960)|January 1, 1972
18-Trisomy in a 15-year-old girlR B Surana, H W Bain, P E Conen
Birth Defects Original Article Series|January 1, 1974
Familial tertiary trisomy with t (14q-; 1 plus?)R B Surana, P E Conen, M Braudo, et al.
Pediatric Cardiology|January 1, 1989
Aortic root dilatation associated with partial trisomy 7(q31.2----qter)K B Roche, J W Moore, R B Surana, et al.
Clinical Genetics|March 1, 1977
46, XY, t(3;22) (p2;q13) resulting in partial trisomy for the short arm of chromosome 3R B Surana, M E Braudo, P E Conen, et al.
Clinical Genetics|June 1, 1995
Constitutional heteromorphism of 9q13 --> q21 in a patient with chronic myelogenous leukemiaR B Surana, S K Rafi, K L Christopher, et al.
American Journal of Medical Genetics|February 2, 1996
Effects of hyperoxia and caffeine on the expression of fragile site at Xq27.3S K Rafi, R B Surana, L H Anderson, et al.
Cytogenetics and Cell Genetics|January 1, 1976
A report on a family with a (1;2) translocation: cytologic and linkage analysisM W Thompson, C T Falk, R G Worton, et al.
Birth Defects Original Article Series|January 11, 1976
A report on a family with a (1;2) translocation: cytologic and linkage analysisM W Thompson, C T Falk, R G Worton, et al.
American Journal of Clinical Pathology|October 1, 1985
Acute myelomonocytic leukemia (M-4 subtype) with abnormal marrow eosinophilia and a normal chromosome 16E W Stark, D F Garvin, R B Surana, et al.
Blood|October 15, 1990
Trisomy 13: a new recurring chromosome abnormality in acute leukemiaH Döhner, D C Arthur, E D Ball, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
American Journal of Diseases of Children (1960)|January 1, 1972
18-Trisomy in a 15-year-old girlR B Surana, H W Bain, P E Conen
Birth Defects Original Article Series|January 1, 1974
Familial tertiary trisomy with t (14q-; 1 plus?)R B Surana, P E Conen, M Braudo, et al.
Pediatric Cardiology|January 1, 1989
Aortic root dilatation associated with partial trisomy 7(q31.2----qter)K B Roche, J W Moore, R B Surana, et al.
Clinical Genetics|March 1, 1977
46, XY, t(3;22) (p2;q13) resulting in partial trisomy for the short arm of chromosome 3R B Surana, M E Braudo, P E Conen, et al.
Clinical Genetics|June 1, 1995
Constitutional heteromorphism of 9q13 --> q21 in a patient with chronic myelogenous leukemiaR B Surana, S K Rafi, K L Christopher, et al.
American Journal of Medical Genetics|February 2, 1996
Effects of hyperoxia and caffeine on the expression of fragile site at Xq27.3S K Rafi, R B Surana, L H Anderson, et al.
Cytogenetics and Cell Genetics|January 1, 1976
A report on a family with a (1;2) translocation: cytologic and linkage analysisM W Thompson, C T Falk, R G Worton, et al.
Birth Defects Original Article Series|January 11, 1976
A report on a family with a (1;2) translocation: cytologic and linkage analysisM W Thompson, C T Falk, R G Worton, et al.
American Journal of Clinical Pathology|October 1, 1985
Acute myelomonocytic leukemia (M-4 subtype) with abnormal marrow eosinophilia and a normal chromosome 16E W Stark, D F Garvin, R B Surana, et al.
Blood|October 15, 1990
Trisomy 13: a new recurring chromosome abnormality in acute leukemiaH Döhner, D C Arthur, E D Ball, et al.
Pageof 2