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Steven R DePalma

Showing results (1-10 of 47) with videos related to

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Human Genetics|December 16, 2003
Localized aggressive periodontitis is linked to human chromosome 1q25Yefu Li, Lin Xu, Hatice Hasturk, et al.
Current Protocols in Molecular Biology|January 13, 2011
Quantification of gene transcripts with deep sequencing analysis of gene expression (DSAGE) using 1 to 2 µg total RNADanos C Christodoulou, Joshua M Gorham, Masataka Kawana, et al.
Stroke|December 10, 2008
Genomewide linkage in a large Caucasian family maps a new locus for intracranial aneurysms to chromosome 13qTeresa Santiago-Sim, Steven R Depalma, Kevin L Ju, et al.
The Annals of Otology, Rhinology, and Laryngology|October 9, 2009
Locus for familial migrainous vertigo disease maps to chromosome 5q35Fayez Bahmad, Steven R DePalma, Saumil N Merchant, et al.
BMC Genetics|May 24, 2006
Phenotype-genotype association grid: a convenient method for summarizing multiple association analysesDaniel Levy, Steven R DePalma, Emelia J Benjamin, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 2012
Spectrum of somatic mitochondrial mutations in five cancersTatianna C Larman, Steven R DePalma, Angela G Hadjipanayis, et al.
BMC Medical Genomics|July 27, 2025
Enrichment of tandem repeat element variants near CHD genes identified by short- and long-read genome sequencingAbhilash Suresh, Sarah U Morton, Daniel Quiat, et al.
Circulation|May 3, 2006
Novel locus for an inherited cardiomyopathy maps to chromosome 7Lei Song, Steven R DePalma, Maria Kharlap, et al.
Scientific Reports|March 7, 2015
NKX2-5 mutations in an inbred consanguineous population: genetic and phenotypic diversityOssama K Abou Hassan, Akl C Fahed, Manal Batrawi, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 7, 2017
Identification of pathogenic gene mutations in <i>LMNA</i> and <i>MYBPC3</i> that alter RNA splicingKaoru Ito, Parth N Patel, Joshua M Gorham, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Human Genetics|December 16, 2003
Localized aggressive periodontitis is linked to human chromosome 1q25Yefu Li, Lin Xu, Hatice Hasturk, et al.
Current Protocols in Molecular Biology|January 13, 2011
Quantification of gene transcripts with deep sequencing analysis of gene expression (DSAGE) using 1 to 2 µg total RNADanos C Christodoulou, Joshua M Gorham, Masataka Kawana, et al.
Stroke|December 10, 2008
Genomewide linkage in a large Caucasian family maps a new locus for intracranial aneurysms to chromosome 13qTeresa Santiago-Sim, Steven R Depalma, Kevin L Ju, et al.
The Annals of Otology, Rhinology, and Laryngology|October 9, 2009
Locus for familial migrainous vertigo disease maps to chromosome 5q35Fayez Bahmad, Steven R DePalma, Saumil N Merchant, et al.
BMC Genetics|May 24, 2006
Phenotype-genotype association grid: a convenient method for summarizing multiple association analysesDaniel Levy, Steven R DePalma, Emelia J Benjamin, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 2012
Spectrum of somatic mitochondrial mutations in five cancersTatianna C Larman, Steven R DePalma, Angela G Hadjipanayis, et al.
BMC Medical Genomics|July 27, 2025
Enrichment of tandem repeat element variants near CHD genes identified by short- and long-read genome sequencingAbhilash Suresh, Sarah U Morton, Daniel Quiat, et al.
Circulation|May 3, 2006
Novel locus for an inherited cardiomyopathy maps to chromosome 7Lei Song, Steven R DePalma, Maria Kharlap, et al.
Scientific Reports|March 7, 2015
NKX2-5 mutations in an inbred consanguineous population: genetic and phenotypic diversityOssama K Abou Hassan, Akl C Fahed, Manal Batrawi, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 7, 2017
Identification of pathogenic gene mutations in <i>LMNA</i> and <i>MYBPC3</i> that alter RNA splicingKaoru Ito, Parth N Patel, Joshua M Gorham, et al.
Pageof 5