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Emergency Medicine Journal : EMJ
|
October 10, 2013
Sustained life-like waveform capnography after human cadaveric tracheal intubation
Cliff 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 results
Mark 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 isoform
Shiwani 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 glaucoma
Marija 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 anomalies
Leisha D Nolen, David Amor, Ashley Haywood, et al.
Page
of 2
Search research articles
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Showing results (11-20 of 15) with videos related to
Sort By:
Page
of 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 intubation
Cliff 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 results
Mark 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 isoform
Shiwani 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 glaucoma
Marija 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 anomalies
Leisha D Nolen, David Amor, Ashley Haywood, et al.
Page
of 2