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Neuroendocrinology|October 29, 2019
Diagnostic Approaches to Neuroendocrine Neoplasms of Unknown Primary SiteAlison May Berner, Christodoulos Pipinikas, Anna Ryan, et al.
Clinical Epigenetics|September 2, 2022
Researcher perspectives on ethics considerations in epigenetics: an international surveyCharles Dupras, Terese Knoppers, Nicole Palmour, et al.
International Journal of Legal Medicine|August 31, 2013
Defining background DNA levels found on the skin of children aged 0-5 yearsEleanor Alison May Graham, William John Watkins, Frank Dunstan, et al.
Clinical Biochemistry|June 6, 2009
Incidence of haemoglobinopathies in various populations - the impact of immigrationShirley Henderson, Adele Timbs, Janice McCarthy, et al.
European Journal of Human Genetics : EJHG|July 24, 2014
EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathiesJoanne Traeger-Synodinos, Cornelis L Harteveld, John M Old, et al.
Haematologica|March 12, 2011
Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemiaCaroline Kannengiesser, Mayka Sanchez, Marion Sweeney, et al.
Journal of Child Neurology|January 19, 2022
Comparison of Cosyntropin, Vigabatrin, and Combination Therapy in New-Onset Infantile Spasms in a Prospective Randomized TrialKelly G Knupp, Jason Coryell, Rani K Singh, et al.
Blood|August 5, 2016
A recurring mutation in the respiratory complex 1 protein NDUFB11 is responsible for a novel form of X-linked sideroblastic anemiaDaniel A Lichtenstein, Andrew W Crispin, Anoop K Sendamarai, et al.
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