Showing results (21-30 of 318) with videos related to
Sort By:
Pageof 32
Mayo Clinic Proceedings|March 22, 2000
von Hippel-Lindau diseaseV Couch, N M Lindor, P S Karnes, et al.Genomics|November 24, 1999
Rothmund-thomson syndrome responsible gene, RECQL4: genomic structure and productsS Kitao, N M Lindor, M Shiratori, et al.The Journal of Molecular Diagnostics : JMD|March 20, 2012
The germline MLH1 K618A variant and susceptibility to Lynch syndrome-associated tumorsFabiola Medeiros, Noralane M Lindor, Fergus J Couch, et al.American Journal of Ophthalmology|March 26, 2003
Unilateral Lisch nodules in the absence of other features of neurofibromatosis 1Garima Lal, Jacqueline A Leavitt, Noralane M Lindor, et al.American Journal of Medical Genetics. Part A|July 24, 2012
Chronic tibial nonunion in a Rothmund-Thomson syndrome patientAaron M Carlson, Kristen B Thomas, Salman Kirmani, et al.American Journal of Medical Genetics|September 19, 1997
Melorheostosis in a patient with familial osteopoikilosisC E Butkus, V V Michels, N M Lindor, et al.Mayo Clinic Proceedings|January 12, 2000
Care of patients and their families with familial adenomatous polyposisJ E King, R R Dozois, N M Lindor, et al.American Journal of Medical Genetics. Part A|June 25, 2004
Nonmosaic smallest duplication of 12q24.31-qter: the first reported caseJulie Won Ireland, Syed M Jalal, Pamela S McGrann, et al.American Journal of Human Genetics|March 23, 2000
Pyogenic arthritis, pyoderma gangrenosum, and acne syndrome maps to chromosome 15qH B Yeon, N M Lindor, J G Seidman, et al.Journal of Neurogenetics|March 26, 2008
Premutations in the FMR1 gene are uncommon in men undergoing genetic testing for spinocerebellar ataxiaSara A Adams, Kelle J Steenblock, Stephen N Thibodeau, et al.Pageof 32