Showing results (681-690 of 5,631) with videos related to
Sort By:
Pageof 564
European Journal of Human Genetics : EJHG|September 11, 2008
Re-assigning the DFNB33 locus to chromosome 10p11.23-q21.1Hanen Belguith, Saber Masmoudi, Myrna Medlej-Hashim, et al.European Journal of Human Genetics : EJHG|September 11, 2008
The E-cadherin (CDH1)--160 C/A polymorphism and prostate cancer risk: a meta-analysisLi-Xin Qiu, Ru-Tian Li, Jian-Bing Zhang, et al.European Journal of Human Genetics : EJHG|February 11, 2010
The USH2A c.2299delG mutation: dating its common origin in a Southern European populationElena Aller, Lise Larrieu, Teresa Jaijo, et al.European Journal of Human Genetics : EJHG|February 11, 2010
Evidence for CTLA4 as a susceptibility gene for dilated cardiomyopathyVolker Ruppert, Thomas Meyer, Clarissa Struwe, et al.European Journal of Human Genetics : EJHG|February 11, 2010
Mammary-digital-nail (MDN) syndrome: a novel phenotype maps to human chromosome 22q12.3-13.1Mira Genzer-Nir, Morad Khayat, Leonid Kogan, et al.European Journal of Human Genetics : EJHG|March 4, 2010
The p.A897KfsX4 frameshift variation in desmocollin-2 is not a causative mutation in arrhythmogenic right ventricular cardiomyopathyMarzia De Bortoli, Giorgia Beffagna, Barbara Bauce, et al.European Journal of Human Genetics : EJHG|June 15, 2018
Knockdown of Crispld2 in zebrafish identifies a novel network for nonsyndromic cleft lip with or without cleft palate candidate genesBrett T Chiquet, Qiuping Yuan, Eric C Swindell, et al.European Journal of Human Genetics : EJHG|June 15, 2018
A heterozygous microdeletion of 20q13.13 encompassing ADNP gene in a child with Helsmoortel-van der Aa syndromeMinh-Tuan Huynh, Elise Boudry-Labis, Alfred Massard, et al.European Journal of Human Genetics : EJHG|June 16, 2018
Cancer prevention by aspirin in children with Constitutional Mismatch Repair Deficiency (CMMRD)Erika K S M Leenders, Harm Westdorp, Roger J Brüggemann, et al.European Journal of Human Genetics : EJHG|June 16, 2018
Utility of two SMN1 variants to improve spinal muscular atrophy carrier diagnosis and genetic counsellingLaura Alías, Sara Bernal, Maite Calucho, et al.Pageof 564