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American Journal of Human Genetics|March 1, 1989
Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90C Robbins, J Theilmann, S Youngman, et al.
British Medical Journal (Clinical Research Ed.)|November 22, 1986
Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophyA L Meredith, S M Huson, P W Lunt, et al.
Brain Research. Molecular Brain Research|June 3, 1999
Localization of rabbit huntingtin using a new panel of monoclonal antibodiesF L Wilkinson, T M Nguyen, S B Manilal, et al.
Journal of Medical Genetics|December 1, 1992
Severity of chest disease in cystic fibrosis patients in relation to their genotypesL N al-Jader, A L Meredith, H C Ryley, et al.
Human Molecular Genetics|July 1, 1993
Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangementsM Upadhyaya, P Jardine, J Maynard, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|December 27, 2008
Ascertaining causes of neonatal deaths using verbal autopsy: current methods and challengesN Thatte, H D Kalter, A H Baqui, et al.
Frontiers in Human Neuroscience|October 30, 2013
Consumption of glucose drinks slows sensorimotor processing: double-blind placebo-controlled studies with the Eriksen flanker taskChristopher Hope, Ellen Seiss, Philip J A Dean, et al.
American Journal of Respiratory and Critical Care Medicine|December 31, 1997
Alveolar and dead space volume measured by oscillations of inspired oxygen in awake adultsE M Williams, R M Hamilton, L Sutton, et al.
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