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A E Bale

Showing results (71-80 of 81) with videos related to

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Genomics|April 1, 1989
Linkage analysis of multiple endocrine neoplasia type 1 with INT2 and other markers on chromosome 11S J Bale, A E Bale, K Stewart, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Regional localization of the selenocysteine tRNA gene (TRSP) on human chromosome 19A Mitchell, A E Bale, B J Lee, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Pulsed-field gel electrophoresis and FISH mapping of chromosome 9q22: placement of a novel zinc finger gene within the NBCCS and ESS1 regionS Levanat, A Chidambaram, C Wicking, et al.
Cytogenetics and Cell Genetics|January 1, 1995
CEPH consortium map of chromosome 14D W Cox, G D Billingsley, A E Bale, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1993
Mutation hotspots due to sunlight in the p53 gene of nonmelanoma skin cancersA Ziegler, D J Leffell, S Kunala, et al.
Cancer Research|February 15, 1991
Allelic loss on chromosome 11 in hereditary and sporadic tumors related to familial multiple endocrine neoplasia type 1A E Bale, J A Norton, E L Wong, et al.
Nature Genetics|September 1, 1996
The role of the human homologue of Drosophila patched in sporadic basal cell carcinomasM R Gailani, M Ståhle-Bäckdahl, D J Leffell, et al.
American Journal of Human Genetics|September 1, 1990
A locus for familial hypertrophic cardiomyopathy is closely linked to the cardiac myosin heavy chain genes, CRI-L436, and CRI-L329 on chromosome 14 at q11-q12S D Solomon, A A Geisterfer-Lowrance, H P Vosberg, et al.
Science (New York, N.Y.)|November 13, 1992
Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22L A Cannon-Albright, D E Goldgar, L J Meyer, et al.
Cell|June 14, 1996
Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndromeH Hahn, C Wicking, P G Zaphiropoulous, et al.
Pageof 9

Showing results (71-80 of 81) with videos related to

Sort By:
Pageof 9
Genomics|April 1, 1989
Linkage analysis of multiple endocrine neoplasia type 1 with INT2 and other markers on chromosome 11S J Bale, A E Bale, K Stewart, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Regional localization of the selenocysteine tRNA gene (TRSP) on human chromosome 19A Mitchell, A E Bale, B J Lee, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Pulsed-field gel electrophoresis and FISH mapping of chromosome 9q22: placement of a novel zinc finger gene within the NBCCS and ESS1 regionS Levanat, A Chidambaram, C Wicking, et al.
Cytogenetics and Cell Genetics|January 1, 1995
CEPH consortium map of chromosome 14D W Cox, G D Billingsley, A E Bale, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1993
Mutation hotspots due to sunlight in the p53 gene of nonmelanoma skin cancersA Ziegler, D J Leffell, S Kunala, et al.
Cancer Research|February 15, 1991
Allelic loss on chromosome 11 in hereditary and sporadic tumors related to familial multiple endocrine neoplasia type 1A E Bale, J A Norton, E L Wong, et al.
Nature Genetics|September 1, 1996
The role of the human homologue of Drosophila patched in sporadic basal cell carcinomasM R Gailani, M Ståhle-Bäckdahl, D J Leffell, et al.
American Journal of Human Genetics|September 1, 1990
A locus for familial hypertrophic cardiomyopathy is closely linked to the cardiac myosin heavy chain genes, CRI-L436, and CRI-L329 on chromosome 14 at q11-q12S D Solomon, A A Geisterfer-Lowrance, H P Vosberg, et al.
Science (New York, N.Y.)|November 13, 1992
Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22L A Cannon-Albright, D E Goldgar, L J Meyer, et al.
Cell|June 14, 1996
Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndromeH Hahn, C Wicking, P G Zaphiropoulous, et al.
Pageof 9