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Scientific Reports|February 4, 2015
Spectrally shaped DP-16QAM super-channel transmission with multi-channel digital back-propagationRobert Maher, Tianhua Xu, Lidia Galdino, et al.Human Genomics|July 24, 2010
Characterisation of a functional intronic polymorphism in the human growth hormone (GH1) geneDavid S Millar, Martin Horan, Nadia A Chuzhanova, et al.Journal of Pediatric Hematology/Oncology|May 22, 2003
Prenatal exclusion of severe factor VII deficiencyHany Ariffin, David S Millar, David N Cooper, et al.Optics Express|April 11, 2014
High-dimensional modulation for coherent optical communications systemsDavid S Millar, Toshiaki Koike-Akino, Sercan Ö Arık, et al.Optics Express|December 31, 2020
Spectrally sparse optical coherence tomographyOkan Atalar, David S Millar, Pu Wang, et al.Genomic Medicine|September 24, 2008
Two sisters with Rett syndrome and non-identical paternally-derived microdeletions in the MECP2 geneLyndon G Rosser, Shane McKee, David S Millar, et al.Human Genomics|September 18, 2010
An isolated case of lissencephaly caused by the insertion of a mitochondrial genome-derived DNA sequence into the 5' untranslated region of the PAFAH1B1 (LIS1) geneDavid S Millar, Carolyn Tysoe, Lazarus P Lazarou, et al.Human Mutation|March 26, 2003
Human growth hormone 1 (GH1) gene expression: complex haplotype-dependent influence of polymorphic variation in the proximal promoter and locus control regionMartin Horan, David S Millar, Jürgen Hedderich, et al.Plos One|December 11, 2013
A nonsense mutation in the IKBKG gene in mares with incontinentia pigmentiRachel E Towers, Leonardo Murgiano, David S Millar, et al.Human Genetics|June 30, 2020
The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research settingPeter D Stenson, Matthew Mort, Edward V Ball, et al.Pageof 4