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S Girirajan

Showing results (1-10 of 7) with videos related to

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Biopolymers|November 1, 1989
Vibrational free energy, entropy, and temperature factors of DNA calculated by a helix lattice approachK S Girirajan, L Young, E W Prohofsky
Journal of Medical Genetics|March 25, 2005
RAI1 variations in Smith-Magenis syndrome patients without 17p11.2 deletionsS Girirajan, L J Elsas, K Devriendt, et al.
Clinical Genetics|February 25, 2009
A functional network module for Smith-Magenis syndromeS Girirajan, H T Truong, C L Blanchard, et al.
Clinical Genetics|June 28, 2007
17p11.2p12 triplication and del(17)q11.2q12 in a severely affected child with dup(17)p11.2p12 syndromeS Girirajan, S R Williams, J Y Garbern, et al.
Journal of Medical Genetics|May 15, 2003
Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in IndiaM RamShankar, S Girirajan, O Dagan, et al.
Clinical Genetics|June 2, 2007
Gender, genotype, and phenotype differences in Smith-Magenis syndrome: a meta-analysis of 105 casesE A Edelman, S Girirajan, B Finucane, et al.
Clinical Genetics|January 23, 2010
Eyebrow anomalies as a diagnostic sign of genomic disordersM Silengo, E Belligni, C Molinatto, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Biopolymers|November 1, 1989
Vibrational free energy, entropy, and temperature factors of DNA calculated by a helix lattice approachK S Girirajan, L Young, E W Prohofsky
Journal of Medical Genetics|March 25, 2005
RAI1 variations in Smith-Magenis syndrome patients without 17p11.2 deletionsS Girirajan, L J Elsas, K Devriendt, et al.
Clinical Genetics|February 25, 2009
A functional network module for Smith-Magenis syndromeS Girirajan, H T Truong, C L Blanchard, et al.
Clinical Genetics|June 28, 2007
17p11.2p12 triplication and del(17)q11.2q12 in a severely affected child with dup(17)p11.2p12 syndromeS Girirajan, S R Williams, J Y Garbern, et al.
Journal of Medical Genetics|May 15, 2003
Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in IndiaM RamShankar, S Girirajan, O Dagan, et al.
Clinical Genetics|June 2, 2007
Gender, genotype, and phenotype differences in Smith-Magenis syndrome: a meta-analysis of 105 casesE A Edelman, S Girirajan, B Finucane, et al.
Clinical Genetics|January 23, 2010
Eyebrow anomalies as a diagnostic sign of genomic disordersM Silengo, E Belligni, C Molinatto, et al.
Pageof 1