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Proceedings of the National Academy of Sciences of the United States of America|May 16, 2012
The polymorphism rs944289 predisposes to papillary thyroid carcinoma through a large intergenic noncoding RNA gene of tumor suppressor typeJaroslaw Jendrzejewski, Huiling He, Hanna S Radomska, et al.
Lancet (London, England)|May 2, 1992
Identical genetic locus for Baltic and Mediterranean myoclonusA Malafosse, A E Lehesjoki, P Genton, et al.
Molecular Vision|August 8, 2007
Study of p.N247S KERA mutation in a British family with cornea planaPetra Liskova, Pirro G Hysi, Denise Williams, et al.
Scientific Reports|July 2, 2025
Brain dynamics of the interplay between auditory selective attention and working memory during melody encodingAurélien de la Chapelle, Salomé Serres-Blain, Alma ElShafei, et al.
Human Mutation|April 29, 1998
Clustering of private mutations in the congenital chloride diarrhea/down-regulated in adenoma geneP Höglund, S Haila, K H Gustavson, et al.
European Journal of Human Genetics : EJHG|February 16, 2006
Phenotypic and genotypic heterogeneity in the Lynch syndrome: diagnostic, surveillance and management implicationsHenry T Lynch, C Richard Boland, Gordon Gong, et al.
Experimental Hematology|October 31, 2003
BAALC, a novel marker of human hematopoietic progenitor cellsClaudia D Baldus, Stephan M Tanner, Donna F Kusewitt, et al.
Thyroid : Official Journal of the American Thyroid Association|January 14, 2020
A Truncating Germline Mutation of <i>TINF2</i> in Individuals with Thyroid Cancer or Melanoma Results in Longer TelomeresHuiling He, Wei Li, Daniel F Comiskey, et al.
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