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Nucleic Acids Research
|
August 25, 1990
Two RFLPs at the glutathione S-transferase 3 gene
E L Wong, G Kandpal, A E Bale
Nucleic Acids Research
|
August 11, 1988
A retinoic acid receptor cDNA probe (RAR2) identifies a moderately frequent RFLP on chromosome 17
A E Bale, C Weinberger, O W McBride
Clinical Chemistry
|
December 1, 1992
DNA diagnosis with mutation-specific artificial methylation sites: application to rapid screening of delta F508
E M Petty, E Gold, A E Bale
Methods in Molecular Medicine
|
March 4, 2011
Direct molecular diagnosis of multiple endocrine neoplasia type 1
E M Petty, M Glynn, A E Bale
Biotechniques
|
August 1, 1995
Direct molecular analysis of archival tumor tissue for loss of heterozygosity
D R Johnson, S Levanat, A E Bale
Nucleic Acids Research
|
February 11, 1991
Ornithine transcarbamylase polymorphism detected by PCR introduction of DraI site
E M Petty, R Carstens, A E Bale
The Journal of Investigative Dermatology
|
November 1, 1994
Nevoid basal cell carcinoma syndrome
A E Bale, M R Gailani, D J Leffell
Genetic Epidemiology. Supplement
|
January 1, 1986
Linkage relationships among four 11p markers in the Utah dataset
S J Bale, E L Harris, A E Bale
Proceedings of the Association of American Physicians
|
July 1, 1995
The Gorlin syndrome gene: a tumor suppressor active in basal cell carcinogenesis and embryonic development
A E Bale, M R Gailani, D J Leffell
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 22, 2001
Medium-chain acyl-CoA dehydrogenase deficiency: sudden and unexpected death of a 45 year old woman
K Raymond, A E Bale, C A Barnes, et al.
Page
of 9
Search research articles
Search
Showing results (11-20 of 81) with videos related to
Sort By:
Page
of 9
Nucleic Acids Research
|
August 25, 1990
Two RFLPs at the glutathione S-transferase 3 gene
E L Wong, G Kandpal, A E Bale
Nucleic Acids Research
|
August 11, 1988
A retinoic acid receptor cDNA probe (RAR2) identifies a moderately frequent RFLP on chromosome 17
A E Bale, C Weinberger, O W McBride
Clinical Chemistry
|
December 1, 1992
DNA diagnosis with mutation-specific artificial methylation sites: application to rapid screening of delta F508
E M Petty, E Gold, A E Bale
Methods in Molecular Medicine
|
March 4, 2011
Direct molecular diagnosis of multiple endocrine neoplasia type 1
E M Petty, M Glynn, A E Bale
Biotechniques
|
August 1, 1995
Direct molecular analysis of archival tumor tissue for loss of heterozygosity
D R Johnson, S Levanat, A E Bale
Nucleic Acids Research
|
February 11, 1991
Ornithine transcarbamylase polymorphism detected by PCR introduction of DraI site
E M Petty, R Carstens, A E Bale
The Journal of Investigative Dermatology
|
November 1, 1994
Nevoid basal cell carcinoma syndrome
A E Bale, M R Gailani, D J Leffell
Genetic Epidemiology. Supplement
|
January 1, 1986
Linkage relationships among four 11p markers in the Utah dataset
S J Bale, E L Harris, A E Bale
Proceedings of the Association of American Physicians
|
July 1, 1995
The Gorlin syndrome gene: a tumor suppressor active in basal cell carcinogenesis and embryonic development
A E Bale, M R Gailani, D J Leffell
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 22, 2001
Medium-chain acyl-CoA dehydrogenase deficiency: sudden and unexpected death of a 45 year old woman
K Raymond, A E Bale, C A Barnes, et al.
Page
of 9