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Clinical Dysmorphology|May 18, 1999
Two brothers with varying combinations of severe developmental delay, epilepsy, microcephaly, tetralogy of Fallot and hydronephrosisA Ryan, J Burn, S Court, et al.Archives of Disease in Childhood. Fetal and Neonatal Edition|July 1, 1996
Natural history of trisomy 18N D Embleton, J P Wyllie, M J Wright, et al.Postgraduate Medical Journal|July 1, 1992
Is bed rest useful after diagnostic lumbar puncture?D A Spriggs, D J Burn, J French, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1991
Lower motor neuron degeneration and familial predisposition to colonic neoplasia in two adult siblingsP J Shaw, P G Ince, J Slade, et al.Gut|December 15, 2000
Colonic crypt cell proliferation state assessed by whole crypt microdissection in sporadic neoplasia and familial adenomatous polyposisS J Mills, J C Mathers, P D Chapman, et al.Pediatric Cardiology|January 1, 1984
Absent right atrioventricular connection and double-inlet ventricle due to an unbalanced familial 8:13 chromosome translocation: a cautionary taleJ Burn, M Baraitser, D T Hughes, et al.Human Mutation|November 25, 2003
Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPAC F Taylor, R S Charlton, J Burn, et al.Parkinsonism & Related Disorders|February 7, 2006
Allelic variation of a functional polymorphism in the serotonin transporter gene and depression in Parkinson's diseaseDavid J Burn, Watcharee Tiangyou, Liesl M Allcock, et al.Annals of Human Genetics|July 1, 1993
Germline rearrangement of MCC and APC detected by pulsed field gel electrophoresis and fluorescent in situ hybridizationS Gayther, D Wells, K Gulati, et al.Movement Disorders : Official Journal of the Movement Disorder Society|February 5, 2009
Levodopa use and sleep in patients with dementia with Lewy bodiesSophie Molloy, Thais Minett, John T O'Brien, et al.Pageof 51