Showing results (31-40 of 46) with videos related to
Sort By:
Pageof 5
Genetic Counseling (Geneva, Switzerland)|July 16, 2008
Sleep problems in individuals with 11q terminal deletion disorder (Jacobsen syndrome)A P H M Maas, P D Grossfeld, R Didden, et al.Carcinogenesis|April 18, 2008
Lack of DNA mismatch repair protein MSH6 in the rat results in hereditary non-polyposis colorectal cancer-like tumorigenesisRuben van Boxtel, Pim W Toonen, Henk S van Roekel, et al.Biotechniques|July 12, 2012
Effective flow cytometric phenotyping of cells using minimal amounts of antibodyDeepak Sharma, Mark R Eichelberg, Jill D Haag, et al.European Neurology|January 1, 1983
Progressive idiopathic strio-pallido-dentate calcinosis (Fahr's disease) with autosomal recessive inheritance. Report of three siblingsM G Smits, F J Gabreëls, H O Thijssen, et al.Journal of Intellectual Disability Research : JIDR|July 20, 2010
Sleep disturbances and behavioural problems in adults with Prader-Willi syndromeA P H M Maas, M Sinnema, R Didden, et al.Acta Neuropathologica|January 1, 1995
Congenital muscular dystrophy and severe central nervous system atrophy in two siblingsQ H Leyten, P G Barth, F J Gabreëls, et al.Genetics|June 21, 2005
Identification of a rat model for usher syndrome type 1B by N-ethyl-N-nitrosourea mutagenesis-driven forward geneticsBart M G Smits, Theo A Peters, Joram D Mul, et al.Bioinformatics (Oxford, England)|February 23, 2013
EBSeq: an empirical Bayes hierarchical model for inference in RNA-seq experimentsNing Leng, John A Dawson, James A Thomson, et al.Pharmacogenetics and Genomics|February 24, 2006
Generation of gene knockouts and mutant models in the laboratory rat by ENU-driven target-selected mutagenesisBart M G Smits, Josine B Mudde, Jose van de Belt, et al.Neuropediatrics|August 1, 1982
Peripheral and central myelinopathy in Cockayne's syndrome. Report of 3 siblingsM G Smits, F J Gabreëls, W O Renier, et al.Pageof 5