Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

F X Arredondo-Vega

Showing results (1-10 of 19) with videos related to

Pageof 2
Sort By:
Journal of Inherited Metabolic Disease|June 1, 1997
Clinical expression, genetics and therapy of adenosine deaminase (ADA) deficiencyM S Hershfield, F X Arredondo-Vega, I Santisteban
Annals of Human Genetics|May 1, 1982
Assignment of the gene for cytosolic alanine aminotransferase (AAT1) to human chromosome 8K H Astrin, F X Arredondo-Vega, R J Desnick, et al.
Somatic Cell Genetics|March 1, 1983
Isolation and characterization of interspecific heat-resistant hybrids between a temperature-sensitive chinese hamster cell asparaginyl-tRNA synthetase mutant and normal human leukocytes: assignment of human asnS gene to chromosome 18R E Cirullo, F X Arredondo-Vega, M Smith, et al.
Somatic Cell Genetics|September 1, 1983
Assignment of structural gene for asparagine synthetase to human chromosome 7S M Arfin, R E Cirullo, F X Arredondo-Vega, et al.
American Journal of Human Genetics|October 3, 1998
Adenosine deaminase deficiency: genotype-phenotype correlations based on expressed activity of 29 mutant allelesF X Arredondo-Vega, I Santisteban, S Daniels, et al.
Cytogenetics and Cell Genetics|January 1, 1982
Regional assignment of the structural gene for human acid beta-glucosidase to q42 leads to qter on chromosome 1E A Devine, M Smith, F X Arredondo-Vega, et al.
Progress in Clinical and Biological Research|January 1, 1982
Chromosomal localization of the gene for Gaucher diseaseE A Devine, M Smith, F X Arredondo-Vega, et al.
Annals of Human Genetics|May 1, 1989
Isozyme and DNA analysis of human S-adenosyl-L-homocysteine hydrolase (AHCY)F X Arredondo-Vega, J A Charlton, Y H Edwards, et al.
The New England Journal of Medicine|May 23, 1996
Brief report: hepatic dysfunction as a complication of adenosine deaminase deficiencyM E Bollinger, F X Arredondo-Vega, I Santisteban, et al.
American Journal of Human Genetics|May 1, 1994
Correct splicing despite mutation of the invariant first nucleotide of a 5' splice site: a possible basis for disparate clinical phenotypes in siblings with adenosine deaminase deficiencyF X Arredondo-Vega, I Santisteban, S Kelly, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Journal of Inherited Metabolic Disease|June 1, 1997
Clinical expression, genetics and therapy of adenosine deaminase (ADA) deficiencyM S Hershfield, F X Arredondo-Vega, I Santisteban
Annals of Human Genetics|May 1, 1982
Assignment of the gene for cytosolic alanine aminotransferase (AAT1) to human chromosome 8K H Astrin, F X Arredondo-Vega, R J Desnick, et al.
Somatic Cell Genetics|March 1, 1983
Isolation and characterization of interspecific heat-resistant hybrids between a temperature-sensitive chinese hamster cell asparaginyl-tRNA synthetase mutant and normal human leukocytes: assignment of human asnS gene to chromosome 18R E Cirullo, F X Arredondo-Vega, M Smith, et al.
Somatic Cell Genetics|September 1, 1983
Assignment of structural gene for asparagine synthetase to human chromosome 7S M Arfin, R E Cirullo, F X Arredondo-Vega, et al.
American Journal of Human Genetics|October 3, 1998
Adenosine deaminase deficiency: genotype-phenotype correlations based on expressed activity of 29 mutant allelesF X Arredondo-Vega, I Santisteban, S Daniels, et al.
Cytogenetics and Cell Genetics|January 1, 1982
Regional assignment of the structural gene for human acid beta-glucosidase to q42 leads to qter on chromosome 1E A Devine, M Smith, F X Arredondo-Vega, et al.
Progress in Clinical and Biological Research|January 1, 1982
Chromosomal localization of the gene for Gaucher diseaseE A Devine, M Smith, F X Arredondo-Vega, et al.
Annals of Human Genetics|May 1, 1989
Isozyme and DNA analysis of human S-adenosyl-L-homocysteine hydrolase (AHCY)F X Arredondo-Vega, J A Charlton, Y H Edwards, et al.
The New England Journal of Medicine|May 23, 1996
Brief report: hepatic dysfunction as a complication of adenosine deaminase deficiencyM E Bollinger, F X Arredondo-Vega, I Santisteban, et al.
American Journal of Human Genetics|May 1, 1994
Correct splicing despite mutation of the invariant first nucleotide of a 5' splice site: a possible basis for disparate clinical phenotypes in siblings with adenosine deaminase deficiencyF X Arredondo-Vega, I Santisteban, S Kelly, et al.
Pageof 2