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Hereditary Cancer in Clinical Practice|May 6, 2011
Primary appendiceal mucinous adenocarcinoma in two first-degree relatives: case report and reviewAdrianne R Racek, Kari G Rabe, Myra J Wick, et al.American Journal of Medical Genetics|November 15, 1994
Sanfilippo syndrome type A in two adult sibsN M Lindor, A Hoffman, J F O'Brien, et al.Journal of the Association of Genetic Technologists|March 7, 2008
Ready reference to common segmental aneusomies by syndromic names, major features and chromosomal locationsElyse B Mitchell, Kimberly Leonhard, Peggy J Stupca, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 11, 2012
Identification of constitutional MLH1 epimutations and promoter variants in colorectal cancer patients from the Colon Cancer Family RegistryRobyn L Ward, Timothy Dobbins, Noralane M Lindor, et al.The Oncologist|April 26, 2013
BRCA1/2 sequence variants of uncertain significance: a primer for providers to assist in discussions and in medical managementNoralane M Lindor, David E Goldgar, Sean V Tavtigian, et al.Clinical Genetics|February 3, 2015
Genetic counselors' practices and confidence regarding variant of uncertain significance results and reclassification from BRCA testingC L Scherr, N M Lindor, T L Malo, et al.Mayo Clinic Proceedings|January 13, 2012
Increased cancer risks in myotonic dystrophyAung Ko Win, Promilla G Perattur, Jose S Pulido, et al.American Journal of Medical Genetics|March 13, 1995
Asplenia in two father-son pairsN M Lindor, W A Smithson, C A Ahumada, et al.Reviews in Cardiovascular Medicine|August 12, 2010
Left ventricular noncompaction cardiomyopathy: what do we know?Timothy E Paterick, Thomas C Gerber, Sala Ray Pradhan, et al.Mayo Clinic Proceedings|January 13, 2001
Application of multicolor fluorescent in situ hybridization for enhanced characterization of chromosomal abnormalities in congenital disordersS M Jalal, M E Law, N M Lindor, et al.Pageof 32