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A E Bale

Showing results (31-40 of 81) with videos related to

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Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|June 1, 1996
Sonographic and DNA-based prenatal detection of Gorlin syndromeB M Petrikovsky, M G Bialer, J A McLaughlin, et al.
Human Mutation|June 30, 2000
Identification of PATCHED mutations in medulloblastomas by direct sequencingJ Dong, M R Gailani, S L Pomeroy, et al.
Nucleic Acids Research|August 11, 1988
A cDNA probe (PheA12) from the hc-(ERBA) gene on chromosome 3 detects a high frequency RFLPA E Bale, S Usala, C Weinberger, et al.
The Laryngoscope|April 14, 1999
Mutational analyses of candidate genes in human squamous cell carcinomasA Petroianu, W L Boson, A E Bale, et al.
The Journal of Pediatrics|September 15, 1999
Familial medullary thyroid carcinoma: presymptomatic diagnosis and management in childrenR A Heptulla, R P Schwartz, A E Bale, et al.
American Journal of Human Genetics|May 1, 1994
Localization of the gene for the nevoid basal cell carcinoma syndromeA M Goldstein, C Stewart, A E Bale, et al.
Lancet (London, England)|August 13, 1994
Prenatal diagnosis of Gorlin syndromeM G Bialer, M R Gailani, J A McLaughlin, et al.
Journal of Dental Research|July 13, 2000
PTCH gene mutations in odontogenic keratocystsD C Barreto, R S Gomez, A E Bale, et al.
Genomics|November 1, 1991
A contiguous linkage map of chromosome 13q with 39 distinct loci separated on average by 5.1 centimorgansA M Bowcock, L A Farrer, J M Hebert, et al.
Cancer Genetics and Cytogenetics|October 15, 1989
Sister chromatid exchange and chromosome fragility in the nevoid basal cell carcinoma syndromeA E Bale, S J Bale, H Murli, et al.
Pageof 9

Showing results (31-40 of 81) with videos related to

Sort By:
Pageof 9
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|June 1, 1996
Sonographic and DNA-based prenatal detection of Gorlin syndromeB M Petrikovsky, M G Bialer, J A McLaughlin, et al.
Human Mutation|June 30, 2000
Identification of PATCHED mutations in medulloblastomas by direct sequencingJ Dong, M R Gailani, S L Pomeroy, et al.
Nucleic Acids Research|August 11, 1988
A cDNA probe (PheA12) from the hc-(ERBA) gene on chromosome 3 detects a high frequency RFLPA E Bale, S Usala, C Weinberger, et al.
The Laryngoscope|April 14, 1999
Mutational analyses of candidate genes in human squamous cell carcinomasA Petroianu, W L Boson, A E Bale, et al.
The Journal of Pediatrics|September 15, 1999
Familial medullary thyroid carcinoma: presymptomatic diagnosis and management in childrenR A Heptulla, R P Schwartz, A E Bale, et al.
American Journal of Human Genetics|May 1, 1994
Localization of the gene for the nevoid basal cell carcinoma syndromeA M Goldstein, C Stewart, A E Bale, et al.
Lancet (London, England)|August 13, 1994
Prenatal diagnosis of Gorlin syndromeM G Bialer, M R Gailani, J A McLaughlin, et al.
Journal of Dental Research|July 13, 2000
PTCH gene mutations in odontogenic keratocystsD C Barreto, R S Gomez, A E Bale, et al.
Genomics|November 1, 1991
A contiguous linkage map of chromosome 13q with 39 distinct loci separated on average by 5.1 centimorgansA M Bowcock, L A Farrer, J M Hebert, et al.
Cancer Genetics and Cytogenetics|October 15, 1989
Sister chromatid exchange and chromosome fragility in the nevoid basal cell carcinoma syndromeA E Bale, S J Bale, H Murli, et al.
Pageof 9