Showing results (901-910 of 5,631) with videos related to

Sort By:
Pageof 564
European Journal of Human Genetics : EJHG|July 7, 2011
Motivators for participation in a whole-genome sequencing study: implications for translational genomics researchFlavia M Facio, Stephanie Brooks, Johanna Loewenstein, et al.
European Journal of Human Genetics : EJHG|November 11, 2011
Preimplantation genetic diagnosis in female and male carriers of reciprocal translocations: clinical outcome until delivery of 312 cyclesKathelijn Keymolen, Catherine Staessen, Willem Verpoest, et al.
European Journal of Human Genetics : EJHG|November 11, 2011
Identification of the first PAR1 deletion encompassing upstream SHOX enhancers in a family with idiopathic short statureSara Benito-Sanz, Miriam Aza-Carmona, Amaya Rodríguez-Estevez, et al.
European Journal of Human Genetics : EJHG|May 17, 2012
Genetic investigation of FOXO3A requires special attention due to sequence homology with FOXO3BFriederike Flachsbart, Michael Möller, Carolin Däumer, et al.
European Journal of Human Genetics : EJHG|May 17, 2012
Association between the 2-bp deletion polymorphism in the duplicated version of the alpha7 nicotinic receptor gene and P50 sensory gatingRachel H Flomen, Madiha Shaikh, Muriel Walshe, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Non-syndromic deafness associated with a mutation and a polymorphism in the mitochondrial 12S ribosomal RNA gene in a large Zairean pedigreeG Matthijs, S Claes, B Longo-Mbenza, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
Yeast artificial chromosome cloning of the Xq13.3-q21.31 region and fine mapping of a deletion associated with choroideremia and nonspecific mental retardationS M van der Maarel, I H Scholten, J A Maat-Kievit, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
Presence of an IDS-related locus (IDS2) in Xq28 complicates the mutational analysis of Hunter syndromeM L Bondeson, H Malmgren, N Dahl, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
Do Basque- and Caucasian-speaking populations share non-Indo-European ancestors?G Bertorelle, J Bertranpetit, F Calafell, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
UHX1 and PCTK1: precise characterisation and localisation within a gene-rich region in Xp11.23 and evaluation as candidate genes for retinal diseases mapped to Xp21.1-p11.2O Brandau, G Nyakatura, K B Jedele, et al.
Pageof 564