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W R Breg

Showing results (51-60 of 87) with videos related to

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Human Genetics|September 19, 1978
Regulation of rRNA gene expression in a human familial 14p+ marker chromosomeD A Miller, W R Breg, D Warburton, et al.
Nucleic Acids Research|April 25, 1985
An anonymous single copy X-chromosome clone, DXS79, from Xq26-Xq28, identifies a moderately frequent RFLP [HGM8 provisional no. DXS79]P D Murphy, J R Kidd, W R Breg, et al.
American Journal of Medical Genetics|February 1, 1991
DNA-based genetic testing in fifty fragile X familiesP D Murphy, M S Watson, L R Shapiro, et al.
Science (New York, N.Y.)|July 16, 1971
Human thymidine kinase gene locus: assignment to chromosome 17 in a hybrid of man and mouse cellsO J Miller, P W Allderdice, D A Miller, et al.
American Journal of Medical Genetics|January 1, 1981
Unusual mosaicism of de novo structural abnormalities and ocular anomalies in a male with 13 trisomy syndromeP C Reardon, R M Greenstein, R O Howard, et al.
American Journal of Medical Genetics|August 1, 1994
FISH diagnosis of partial trisomy 13 and tetrasomy 13 in a patient with severe trigonocephaly (C) phenotypeT W Chu, A S Teebi, L Gibson, et al.
American Journal of Medical Genetics|May 1, 1986
Chromosome deletion 1q42-43M S Watson, J J Gargus, K J Blakemore, et al.
Nature Genetics|November 1, 1994
Xq-Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotypeB T Lahn, N Ma, W R Breg, et al.
Cytogenetics and Cell Genetics|January 1, 1984
NRAS transforming gene maps to region p11----p13 on chromosome 1 by in situ hybridizationM Rabin, M Watson, P E Barker, et al.
The American Journal of Medicine|August 1, 1979
Angioimmunoblastic lymphadenopathy evolution to a Burkitt-like lymphomaE M Mazur, D H Lovett, R E Enriquez, et al.
Pageof 9

Showing results (51-60 of 87) with videos related to

Sort By:
Pageof 9
Human Genetics|September 19, 1978
Regulation of rRNA gene expression in a human familial 14p+ marker chromosomeD A Miller, W R Breg, D Warburton, et al.
Nucleic Acids Research|April 25, 1985
An anonymous single copy X-chromosome clone, DXS79, from Xq26-Xq28, identifies a moderately frequent RFLP [HGM8 provisional no. DXS79]P D Murphy, J R Kidd, W R Breg, et al.
American Journal of Medical Genetics|February 1, 1991
DNA-based genetic testing in fifty fragile X familiesP D Murphy, M S Watson, L R Shapiro, et al.
Science (New York, N.Y.)|July 16, 1971
Human thymidine kinase gene locus: assignment to chromosome 17 in a hybrid of man and mouse cellsO J Miller, P W Allderdice, D A Miller, et al.
American Journal of Medical Genetics|January 1, 1981
Unusual mosaicism of de novo structural abnormalities and ocular anomalies in a male with 13 trisomy syndromeP C Reardon, R M Greenstein, R O Howard, et al.
American Journal of Medical Genetics|August 1, 1994
FISH diagnosis of partial trisomy 13 and tetrasomy 13 in a patient with severe trigonocephaly (C) phenotypeT W Chu, A S Teebi, L Gibson, et al.
American Journal of Medical Genetics|May 1, 1986
Chromosome deletion 1q42-43M S Watson, J J Gargus, K J Blakemore, et al.
Nature Genetics|November 1, 1994
Xq-Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotypeB T Lahn, N Ma, W R Breg, et al.
Cytogenetics and Cell Genetics|January 1, 1984
NRAS transforming gene maps to region p11----p13 on chromosome 1 by in situ hybridizationM Rabin, M Watson, P E Barker, et al.
The American Journal of Medicine|August 1, 1979
Angioimmunoblastic lymphadenopathy evolution to a Burkitt-like lymphomaE M Mazur, D H Lovett, R E Enriquez, et al.
Pageof 9