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European Child & Adolescent Psychiatry|January 1, 1997
Functional evidence of brain stem immaturity in Rett syndromeP O Julu, A M Kerr, S Hansen, et al.Journal of Medical Genetics|March 21, 1998
"Cataplexy" and muscle ultrasound abnormalities in Coffin-Lowry syndromeY J Crow, S M Zuberi, R McWilliam, 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.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.Archives of Disease in Childhood|May 1, 1996
The changing clinical pattern of Reye's syndrome 1982-1990R M Hardie, L H Newton, J C Bruce, et al.American Journal of Medical Genetics|April 1, 1989
Detection of a 15q deletion in a child with Angelman syndrome by cytogenetic analysis and flow cytometryA Cooke, J L Tolmie, F J Glencross, 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.Archives of Disease in Childhood|November 1, 1994
Diagnosis in Prader-Willi syndromeC E Chu, A Cooke, J B Stephenson, et al.Human Genetics|June 1, 1986
Duchenne muscular dystrophy due to familial Xp21 deletion detectable by DNA analysis and flow cytometryD E Wilcox, A Cooke, J Colgan, et al.Pageof 9