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Journal of Medical Genetics|December 1, 1992
Presymptomatic diagnosis of von Hippel-Lindau disease with flanking DNA markersE R Maher, E Bentley, S J Payne, et al.Human Molecular Genetics|June 1, 1994
Molecular genetic analysis of the 3p- syndromeM E Phipps, F Latif, A Prowse, et al.Journal of Medical Genetics|August 1, 1993
Evaluation of molecular genetic diagnosis in the management of familial adenomatous polyposis coli: a population based studyE R Maher, D E Barton, R Slatter, et al.Archives of Disease in Childhood|April 1, 1993
Cystic fibrosis identified by neonatal screening: incidence, genotype, and early natural historyM R Green, L T Weaver, A F Heeley, et al.BMC Public Health|October 22, 2021
Digital messaging to support control for type 2 diabetes (StAR2D): a multicentre randomised controlled trialA Farmer, K Bobrow, N Leon, et al.NMR in Biomedicine|June 11, 2014
Comparing different analysis methods for quantifying the MRI amide proton transfer (APT) effect in hyperacute stroke patientsY K Tee, G W J Harston, N Blockley, et al.Journal of Medical Genetics|February 1, 1996
A genetic register for von Hippel-Lindau diseaseI R Maddock, A Moran, E R Maher, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 7, 2007
Multiple mitochondrial DNA deletions in monozygotic twins with OPMDM M K Muqit, A J Larner, M G Sweeney, et al.Journal of Medical Genetics|May 8, 2007
Biallelic mutation of MSH2 in primary human cells is associated with sensitivity to irradiation and altered RAD51 foci kineticsJ Barwell, L Pangon, S Hodgson, et al.BMC Cardiovascular Disorders|December 28, 2024
Self-monitoring of blood pressure following a stroke or transient ischaemic attack (TASMIN5S): a randomised controlled trialR J McManus, A Smith, E Temple, et al.Pageof 10