Showing results (371-380 of 510) with videos related to
Sort By:
Pageof 51
American Journal of Human Genetics|May 11, 2005
Homozygous nonsense mutations in KIAA1279 are associated with malformations of the central and enteric nervous systemsAlice S Brooks, Aida M Bertoli-Avella, Grzegorz M Burzynski, et al.Circulation. Cardiovascular Genetics|December 25, 2009
A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN projectFabio Marroni, Arne Pfeufer, Yurii S Aulchenko, et al.Journal of Alzheimer'S Disease : JAD|July 9, 2009
A study of the SORL1 gene in Alzheimer's disease and cognitive functionFan Liu, M Arfan Ikram, A Cecile J W Janssens, et al.Proceedings of the National Academy of Sciences of the United States of America|May 29, 2002
Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactylyLaura A Lettice, Taizo Horikoshi, Simon J H Heaney, et al.Human Molecular Genetics|March 11, 1999
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's DiseaseN Abbas, C B Lücking, S Ricard, et al.Investigative Ophthalmology & Visual Science|January 24, 2012
A genetic epidemiologic study of candidate genes involved in the optic nerve head morphologyAndrea C Gasten, Wishal D Ramdas, Linda Broer, et al.BMC Medical Genomics|March 7, 2018
A combined linkage, microarray and exome analysis suggests MAP3K11 as a candidate gene for left ventricular hypertrophyClaudia Tamar Silva, Irina V Zorkoltseva, Maartje N Niemeijer, et al.Neuron|August 2, 2005
Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in Fragile X syndromeS K E Koekkoek, K Yamaguchi, B A Milojkovic, et al.Kidney International|April 24, 2009
Genome-wide linkage analysis of serum creatinine in three isolated European populationsCristian Pattaro, Yurii S Aulchenko, Aaron Isaacs, et al.Journal of Medical Genetics|November 10, 2010
Genetic architecture of open angle glaucoma and related determinantsWishal D Ramdas, Najaf Amin, Leonieke M E van Koolwijk, et al.Pageof 51