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A E Bale

Showing results (41-50 of 81) with videos related to

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Nature Genetics|January 1, 1996
A two-hit model for developmental defects in Gorlin syndromeS Levanat, R J Gorlin, S Fallet, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
Prenatal molecular diagnosis of severe ornithine carbamoyltransferase deficiency due to a novel mutation, E181GA K Topaloglu, C Sansaricq, J E Fox, et al.
American Journal of Human Genetics|June 1, 1994
Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from NewfoundlandE M Petty, J S Green, S J Marx, et al.
Journal of the National Cancer Institute|March 20, 1996
Relationship between sunlight exposure and a key genetic alteration in basal cell carcinomaM R Gailani, D J Leffell, A Ziegler, et al.
Genes, Chromosomes & Cancer|March 1, 1997
Characterization of a YAC contig containing the NBCCS locus and a novel Kruppel-type zinc finger sequence on chromosome segment 9q22.3A Chidambaram, M Gailani, B Gerrard, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1991
PRAD1, a candidate BCL1 oncogene: mapping and expression in centrocytic lymphomaC L Rosenberg, E Wong, E M Petty, et al.
Genomics|December 1, 1991
Localization of a DNA segment encompassing four tRNA genes to human chromosome 14q11 and its use as an anchor locus for linkage analysisA Mitchell, A E Bale, M Wang-Ge, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1993
Progression of uremic hyperparathyroidism involves allelic loss on chromosome 11A Falchetti, A E Bale, A Amorosi, et al.
Journal of Cutaneous Pathology|January 12, 2007
Congenital linear unilateral basal cell nevus: a case report with patched gene molecular studiesL L Brailey, T Davis, S E Kolker, et al.
The British Journal of Dermatology|July 26, 2014
Alcohol intake and early-onset basal cell carcinoma in a case-control studyY Zhang, L M Ferrucci, B Cartmel, et al.
Pageof 9

Showing results (41-50 of 81) with videos related to

Sort By:
Pageof 9
Nature Genetics|January 1, 1996
A two-hit model for developmental defects in Gorlin syndromeS Levanat, R J Gorlin, S Fallet, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
Prenatal molecular diagnosis of severe ornithine carbamoyltransferase deficiency due to a novel mutation, E181GA K Topaloglu, C Sansaricq, J E Fox, et al.
American Journal of Human Genetics|June 1, 1994
Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from NewfoundlandE M Petty, J S Green, S J Marx, et al.
Journal of the National Cancer Institute|March 20, 1996
Relationship between sunlight exposure and a key genetic alteration in basal cell carcinomaM R Gailani, D J Leffell, A Ziegler, et al.
Genes, Chromosomes & Cancer|March 1, 1997
Characterization of a YAC contig containing the NBCCS locus and a novel Kruppel-type zinc finger sequence on chromosome segment 9q22.3A Chidambaram, M Gailani, B Gerrard, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1991
PRAD1, a candidate BCL1 oncogene: mapping and expression in centrocytic lymphomaC L Rosenberg, E Wong, E M Petty, et al.
Genomics|December 1, 1991
Localization of a DNA segment encompassing four tRNA genes to human chromosome 14q11 and its use as an anchor locus for linkage analysisA Mitchell, A E Bale, M Wang-Ge, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1993
Progression of uremic hyperparathyroidism involves allelic loss on chromosome 11A Falchetti, A E Bale, A Amorosi, et al.
Journal of Cutaneous Pathology|January 12, 2007
Congenital linear unilateral basal cell nevus: a case report with patched gene molecular studiesL L Brailey, T Davis, S E Kolker, et al.
The British Journal of Dermatology|July 26, 2014
Alcohol intake and early-onset basal cell carcinoma in a case-control studyY Zhang, L M Ferrucci, B Cartmel, et al.
Pageof 9