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Iris L Gonzalez

Showing results (1-10 of 9) with videos related to

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American Journal of Medical Genetics. Part A|March 29, 2005
Barth syndrome: TAZ gene mutations, mRNAs, and evolutionIris L Gonzalez
Molecular Genetics and Metabolism|December 18, 2013
Tafazzin splice variants and mutations in Barth syndromeSusan M Kirwin, Athena Manolakos, Sarah Swain Barnett, et al.
Human Mutation|July 13, 2006
Paternal bias in parental origin of HRAS mutations in Costello syndromeKatia Sol-Church, Deborah L Stabley, Linda Nicholson, et al.
Fertility and Sterility|January 24, 2007
Multiple transmissions of Barth syndrome through an oocyte donor with a de novo TAZ mutationSusan M Kirwin, Kathy M Vinette, Sharon B Schwartz, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
A homozygous double mutation in SMN1: a complicated genetic diagnosis of SMASusan M Kirwin, Kathy M B Vinette, Iris L Gonzalez, et al.
Pediatrics|July 19, 2006
Cardiac and clinical phenotype in Barth syndromeCarolyn T Spencer, Randall M Bryant, Jane Day, et al.
American Journal of Medical Genetics. Part A|December 6, 2005
HRAS mutation analysis in Costello syndrome: genotype and phenotype correlationKaren W Gripp, Angela E Lin, Deborah L Stabley, et al.
JIMD Reports|April 23, 2013
A Novel Exonic Splicing Mutation in the TAZ (G4.5) Gene in a Case with Atypical Barth SyndromeYuxin Fan, Jon Steller, Iris L Gonzalez, et al.
Orphanet Journal of Rare Diseases|February 13, 2013
Barth syndromeSarah L N Clarke, Ann Bowron, Iris L Gonzalez, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|March 29, 2005
Barth syndrome: TAZ gene mutations, mRNAs, and evolutionIris L Gonzalez
Molecular Genetics and Metabolism|December 18, 2013
Tafazzin splice variants and mutations in Barth syndromeSusan M Kirwin, Athena Manolakos, Sarah Swain Barnett, et al.
Human Mutation|July 13, 2006
Paternal bias in parental origin of HRAS mutations in Costello syndromeKatia Sol-Church, Deborah L Stabley, Linda Nicholson, et al.
Fertility and Sterility|January 24, 2007
Multiple transmissions of Barth syndrome through an oocyte donor with a de novo TAZ mutationSusan M Kirwin, Kathy M Vinette, Sharon B Schwartz, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
A homozygous double mutation in SMN1: a complicated genetic diagnosis of SMASusan M Kirwin, Kathy M B Vinette, Iris L Gonzalez, et al.
Pediatrics|July 19, 2006
Cardiac and clinical phenotype in Barth syndromeCarolyn T Spencer, Randall M Bryant, Jane Day, et al.
American Journal of Medical Genetics. Part A|December 6, 2005
HRAS mutation analysis in Costello syndrome: genotype and phenotype correlationKaren W Gripp, Angela E Lin, Deborah L Stabley, et al.
JIMD Reports|April 23, 2013
A Novel Exonic Splicing Mutation in the TAZ (G4.5) Gene in a Case with Atypical Barth SyndromeYuxin Fan, Jon Steller, Iris L Gonzalez, et al.
Orphanet Journal of Rare Diseases|February 13, 2013
Barth syndromeSarah L N Clarke, Ann Bowron, Iris L Gonzalez, et al.
Pageof 1