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Clinical Dysmorphology|January 1, 1992
Acrorenal syndrome: further observationsR Houlston, K MacDermotGut|March 28, 2008
Association between chromosomal instability and prognosis in colorectal cancer: a meta-analysisA Walther, R Houlston, I TomlinsonDisease Markers|November 1, 1991
Polymorphisms of the apolipoprotein B and E genes and their possible roles in familial and non-familial combined hyperlipidaemiaR Houlston, B Lewis, S E HumphriesEuropean Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|May 20, 2008
Pseudoaneurysm of the peroneal artery: presentation of Ehlers-Danlos syndrome type IVK Mandeville, C Bicknell, T Tran, et al.Journal of the Royal Society of Medicine|May 1, 1988
Gemfibrozil in the treatment of resistant familial hypercholesterolaemia and type III hyperlipoproteinaemiaR Houlston, J Quiney, G F Watts, et al.Pediatric Nephrology (Berlin, Germany)|July 1, 1987
Anderson-Fabry disease--family linkage studies using two polymorphic X-linked DNA probesS H Morgan, J K Cheshire, T M Wilson, et al.Clinical Dysmorphology|April 1, 1992
Microcephaly, focal segmental glomerulonephritis and marfanoid habitus in two sibsR S Houlston, S Iraggori, V Murday, et al.The British Journal of Dermatology|January 1, 1992
Cancer family syndrome associated with multiple malignant melanomas and a malignant fibrous histiocytomaC Buckley, V Thomas, J Crow, et al.Clinical Genetics|December 1, 1994
Association between genetic variation at the APO AI-CIII-AIV gene cluster and familial combined hyperlipidaemiaC F Xu, P Talmud, H Schuster, et al.Cancer Letters|March 29, 2000
Prevalence of the APC E1317Q variant in colorectal cancer patientsS Popat, J Stone, G Coleman, et al.Pageof 5