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Leukemia|July 1, 2017
SETD2 and histone H3 lysine 36 methylation deficiency in advanced systemic mastocytosisG Martinelli, M Mancini, C De Benedittis, et al.
Journal of the American College of Cardiology|May 18, 2019
Pacemaker Implantation After Mitral Valve Surgery With Atrial Fibrillation AblationJoseph J DeRose, Donna M Mancini, Helena L Chang, et al.
Human Mutation|February 1, 2011
MLL2 mutation spectrum in 45 patients with Kabuki syndromeAimée D C Paulussen, Alexander P A Stegmann, Marinus J Blok, et al.
Circulation. Heart Failure|April 5, 2021
Characteristics and Outcomes of COVID-19 in Patients on Left Ventricular Assist Device SupportEdo Y Birati, Samer S Najjar, Ryan J Tedford, et al.
American Journal of Human Genetics|February 3, 2016
De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital MalformationsMargot R F Reijnders, Vasilios Zachariadis, Brooke Latour, et al.
European Journal of Human Genetics : EJHG|June 10, 2010
The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genesAimée D C Paulussen, Constance T Schrander-Stumpel, Demis C J Tserpelis, et al.
Journal of Medical Genetics|May 7, 2013
Phenotype and genotype in 101 males with X-linked creatine transporter deficiencyJ M van de Kamp, O T Betsalel, S Mercimek-Mahmutoglu, et al.
Cancer Research|March 9, 2005
Large-scale transcriptome analyses reveal new genetic marker candidates of head, neck, and thyroid cancerEduardo M Reis, Elida P B Ojopi, Fernando L Alberto, et al.
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