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Journal of Mental Deficiency Research|December 1, 1988
A low-cost method for simultaneous video-recording of ambulant subject and electroencephalograph: the Quarrier's systemA M Kerr, P M Amos, A H Etchells, et al.Human Molecular Genetics|April 18, 2000
Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and locationJ P Cheadle, H Gill, N Fleming, et al.Archives of Disease in Childhood|June 23, 2001
Characterisation of breathing and associated central autonomic dysfunction in the Rett disorderP O Julu, A M Kerr, F Apartopoulos, et al.Neurology|July 13, 2006
Early progressive encephalopathy in boys and MECP2 mutationsP Kankirawatana, H Leonard, C Ellaway, et al.Journal of Intellectual Disability Research : JIDR|January 25, 2003
Medical needs of people with intellectual disability require regular reassessment, and the provision of client- and carer-held reportsA M Kerr, D McCulloch, K Oliver, et al.American Journal of Human Genetics|October 27, 1997
A spectrum of mutations in the second gene for autosomal dominant polycystic kidney disease (PKD2)B Veldhuisen, J J Saris, S de Haij, et al.Journal of Evolutionary Biology|January 8, 2009
Lovesick: immunological costs of mating to male sagebrush cricketsJ C Leman, C B Weddle, S N Gershman, et al.Journal of Neurology|November 7, 2002
Episodic ataxia type 2. Three novel truncating mutations and one novel missense mutation in the CACNA1A geneA M J M van den Maagdenberg, E E Kors, E R Brunt, et al.Kidney International|April 12, 2000
Location of mutations within the PKD2 gene influences clinical outcomeN Hateboer, B Veldhuisen, D Peters, 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 8