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Neuropsychobiology|March 20, 2010
Spatial learning and expression patterns of PP1 mRNA in mouse hippocampusS Haege, D Galetzka, U Zechner, et al.Cytogenetics and Cell Genetics|January 1, 1997
Identification of positional candidates for neurological disorders on chromsome 13q14-->q22H G Nothwang, J Wirth, B Brandl, et al.Human Molecular Genetics|December 26, 2001
Genome-wide methylation patterns in normal and uniparental early mouse embryosS C Barton, K L Arney, W Shi, et al.Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|February 5, 2011
Methylation status of imprinted genes and repetitive elements in sperm DNA from infertile malesN El Hajj, U Zechner, E Schneider, et al.Journal of Thrombosis and Haemostasis : JTH|July 2, 2013
Deep intronic 'mutations' cause hemophilia A: application of next generation sequencing in patients without detectable mutation in F8 cDNAB Pezeshkpoor, N Zimmer, N Marquardt, et al.Cytogenetic and Genome Research|November 17, 2004
Genomic structure and paralogous regions of the inversion breakpoint occurring between human chromosome 3p12.3 and orangutan chromosome 2Y Yue, B Grossmann, E Tsend-Ayush, et al.Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|October 9, 1999
Somatic pairing between subtelomeric chromosome regions: implications for human genetic disease?K Stout, S van der Maarel, R R Frants, et al.Journal of Medical Genetics|May 24, 2005
Disruption of TCBA1 associated with a de novo t(1;6)(q32.2;q22.3) presenting in a child with developmental delay and recurrent infectionsY Yue, K Stout, B Grossmann, et al.Cytogenetics and Cell Genetics|February 22, 2002
Comparative mapping of the human 9q34 region in Fugu rubripesN Bouchireb, F Grützner, T Haaf, et al.Developmental Biology|February 1, 1985
Developmental acquisition of type X collagen in the embryonic chick tibiotarsusT M Schmid, T F LinsenmayerPageof 191