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Human Molecular Genetics|July 1, 1994
Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cellsJ P Rossiter, M Young, M L Kimberland, et al.Scandinavian Journal of Rheumatology|January 1, 1997
Correlates of disablement in systemic onset juvenile chronic arthritis. A cross sectional studyJ van der Net, W Kuis, A B Prakken, et al.Journal of Medical Genetics|August 1, 1996
Complex genetic predisposition to cancer in an extended HNPCC family with an ancestral hMLH1 mutationP Hutter, A Couturier, R J Scott, et al.Swiss Surgery = Schweizer Chirurgie = Chirurgie Suisse = Chirurgia Svizzera|June 16, 2001
[Multidisciplinary management of hereditary colorectal cancer]C Soravia, C Delozier-Blanchet, J L Blouin, et al.Journal of Medical Genetics|May 16, 2002
An MLH1 haplotype is over-represented on chromosomes carrying an HNPCC predisposing mutation in MLH1P Hutter, J Wijnen, C Rey-Berthod, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 31, 2002
Revision of the American Joint Committee on Cancer staging system for breast cancerS Eva Singletary, Craig Allred, Pandora Ashley, et al.The Surgical Clinics of North America|July 24, 2003
Staging system for breast cancer: revisions for the 6th edition of the AJCC Cancer Staging ManualS Eva Singletary, Craig Allred, Pandora Ashley, et al.Gut|February 8, 2006
Disease severity and genetic pathways in attenuated familial adenomatous polyposis vary greatly but depend on the site of the germline mutationO M Sieber, S Segditsas, A L Knudsen, et al.Environment International|January 2, 2022
Wireless phone use in childhood and adolescence and neuroepithelial brain tumours: Results from the international MOBI-Kids studyG Castaño-Vinyals, S Sadetzki, R Vermeulen, et al.Pageof 5