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Frank Billson

Showing results (11-20 of 15) with videos related to

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Emergency Medicine Journal : EMJ|October 10, 2013
Sustained life-like waveform capnography after human cadaveric tracheal intubationCliff Reid, Anthony Lewis, Karel Habig, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 14, 2003
A randomized clinical trial of a single dose of intravitreal triamcinolone acetonide for neovascular age-related macular degeneration: one-year resultsMark C Gillies, Judy M Simpson, Wei Luo, et al.
Molecular Vision|October 25, 2008
Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoformShiwani Sharma, Kathryn P Burdon, Alpana Dave, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|July 22, 2008
Chromosomal rearrangements and novel genes in disorders of eye development, cataract and glaucomaMarija Mihelec, Luke St Heaps, Maree Flaherty, et al.
American Journal of Medical Genetics. Part A|July 13, 2006
Deletion at 14q22-23 indicates a contiguous gene syndrome comprising anophthalmia, pituitary hypoplasia, and ear anomaliesLeisha D Nolen, David Amor, Ashley Haywood, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Emergency Medicine Journal : EMJ|October 10, 2013
Sustained life-like waveform capnography after human cadaveric tracheal intubationCliff Reid, Anthony Lewis, Karel Habig, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 14, 2003
A randomized clinical trial of a single dose of intravitreal triamcinolone acetonide for neovascular age-related macular degeneration: one-year resultsMark C Gillies, Judy M Simpson, Wei Luo, et al.
Molecular Vision|October 25, 2008
Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoformShiwani Sharma, Kathryn P Burdon, Alpana Dave, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|July 22, 2008
Chromosomal rearrangements and novel genes in disorders of eye development, cataract and glaucomaMarija Mihelec, Luke St Heaps, Maree Flaherty, et al.
American Journal of Medical Genetics. Part A|July 13, 2006
Deletion at 14q22-23 indicates a contiguous gene syndrome comprising anophthalmia, pituitary hypoplasia, and ear anomaliesLeisha D Nolen, David Amor, Ashley Haywood, et al.
Pageof 2