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Pancreas|September 20, 2011
Pancreatic cancer and a novel MSH2 germline alterationNoralane M Lindor, Gloria M Petersen, Amanda B Spurdle, et al.Clinical Genetics|October 1, 1993
Mosaic trisomy 16 in a thriving infant: maternal heterodisomy for chromosome 16N M Lindor, S M Jalal, S N Thibodeau, et al.Public Health Genomics|March 21, 2015
Public perceptions of disease severity but not actionability correlate with interest in receiving genomic results: nonalignment with current trends in practiceKristi D Graves, Pamela S Sinicrope, Jennifer B McCormick, et al.Nature Genetics|May 13, 1999
Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndromeS Kitao, A Shimamoto, M Goto, et al.American Journal of Medical Genetics|June 19, 1995
Central pontine myelinolysis as a complication of partial ornithine carbamoyl transferase deficiencyL R Mattson, N M Lindor, D H Goldman, et al.Journal of Community Genetics|November 11, 2017
From the laboratory to the clinic: sharing BRCA VUS reclassification tools with practicing genetics professionalsBianca M Augusto, Paige Lake, Courtney L Scherr, et al.Hereditary Cancer in Clinical Practice|March 11, 2014
Colorectal cancer and self-reported tooth agenesisNoralane M Lindor, Aung Ko Win, Steven Gallinger, et al.Mayo Clinic Proceedings|May 1, 1997
Genetic testing in medullary thyroid carcinoma syndromes: mutation types and clinical significanceH M Heshmati, H Gharib, S Khosla, et al.American Journal of Otolaryngology|May 6, 2015
Myhre-LAPs syndrome and intubation related airway stenosis: keys to diagnosis and critical therapeutic interventionsMichael S Oldenburg, Christopher D Frisch, Noralane M Lindor, et al.Mayo Clinic Proceedings|August 1, 1992
A genetic review of complete and partial hydatidiform moles and nonmolar triploidyN M Lindor, J A Ney, T A Gaffey, et al.Pageof 32