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Journal of Medical Genetics|June 4, 1998
Autosomal dominant juvenile recurrent parotitisE Reid, F Douglas, Y Crow, et al.Journal of Medical Genetics|October 5, 2001
Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36D J Hampshire, E Roberts, Y Crow, et al.Life Sciences|February 9, 2005
Modulation of alpha4 integrin mRNA levels is coupled to deficits in vasomotor function in rat arterioles by allylamineJessemy D Neiger, Tracy Y Crow, Charles R Partridge, et al.Journal of Medical Genetics|October 4, 2002
Autosomal recessive primary microcephaly: an analysis of locus heterogeneity and phenotypic variationE Roberts, D J Hampshire, L Pattison, et al.Neuropediatrics|December 3, 2011
COL4A1 mutations associated with a characteristic pattern of intracranial calcificationJ Livingston, D Doherty, S Orcesi, et al.Journal of Medical Genetics|March 16, 2007
Reduced penetrance alleles for Huntington's disease: a multi-centre direct observational studyOliver W J Quarrell, Alan S Rigby, L Barron, et al.Journal of Medical Genetics|September 27, 2005
Gross rearrangements of the MECP2 gene are found in both classical and atypical Rett syndrome patientsH L Archer, S D Whatley, J C Evans, et al.Pageof 1