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Lancet (London, England)|November 28, 1992
Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney diseaseD Ravine, R G Walker, R N Gibson, et al.Nature Genetics|December 1, 1993
Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney diseaseD J Peters, L Spruit, J J Saris, et al.European Child & Adolescent Psychiatry|January 1, 1997
Rett syndrome: analysis of deaths in the British surveyA M Kerr, D D Armstrong, R J Prescott, et al.Journal of Intellectual Disability Research : JIDR|April 25, 2006
People with MECP2 mutation-positive Rett disorder who converseA M Kerr, H L Archer, J C Evans, et al.Clinical Genetics|December 21, 2011
What does the nature of the MECP2 mutation tell us about parental origin and recurrence risk in Rett syndrome?J Zhang, X Bao, G Cao, et al.Journal of Medical Genetics|November 17, 2009
Updating the profile of C-terminal MECP2 deletions in Rett syndromeA Bebbington, A Percy, J Christodoulou, et al.British Journal of Cancer|September 1, 1986
The effect of adriamycin and 4'-deoxydoxorubicin on cell survival of human lung tumour cells grown in monolayer and as spheroidsD J Kerr, T E Wheldon, A M Kerr, et al.Translational Psychiatry|June 4, 2014
Towards a molecular characterization of autism spectrum disorders: an exome sequencing and systems approachJ Y An, A S Cristino, Q Zhao, et al.Archives of Disease in Childhood|September 1, 1988
Hyperventilation in the awake state: potentially treatable component of Rett syndromeD P Southall, A M Kerr, E Tirosh, et al.Journal of Intellectual Disability Research : JIDR|January 25, 2003
Motion analysis of stereotyped hand movements in Rett syndromeM Wright, M L Van der Linden, A M Kerr, et al.Pageof 8