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Cancer Genetics|September 18, 2022
Somatic tumor mutations in moderate risk cancer genes: Targets for germline confirmatory testingHannah Llorin, Madeline Graf, Nicolette Chun, et al.Journal of Genetic Counseling|May 4, 2019
Understanding variants of uncertain significance in the era of multigene panels: Through the eyes of the patientChloe Reuter, Nicolette Chun, Mitchel Pariani, et al.Cancer Genetics|March 14, 2022
Somatic tumor testing implications for Lynch syndrome germline genetic testingKathleen Barrus, Natasha Purington, Nicolette Chun, et al.JNCI Cancer Spectrum|April 8, 2020
Germline Testing for Patients With <i>BRCA1/2</i> Mutations on Somatic Tumor TestingKatherine Vlessis, Natasha Purington, Nicolette Chun, et al.Journal of Genetic Counseling|March 20, 2024
Family health beliefs and cascade genetic testing in Asian families with hereditary cancer risk: "Okay, now what?"Leena Tran, Jennifer L Young, Claire M Barton, et al.JBMR Plus|December 16, 2024
<i>CDC73</i> c.1155-3A>G is a pathogenic variant that causes aberrant splicing, disrupted parafibromin expression, and hyperparathyroidism-jaw tumor syndromeLeor Needleman, Nicolette Chun, Sathvika Sitaraman, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 17, 2007
Identification of an intronic single nucleotide polymorphism leading to allele dropout during validation of a CDH1 sequencing assay: implications for designing polymerase chain reaction-based assaysFranklin M Mullins, Lisa Dietz, Marla Lay, et al.Pediatric Blood & Cancer|June 8, 2007
Identification of a novel p53 in-frame deletion in a Li-Fraumeni-like familyJoshua D Schiffman, Nicolette Chun, Paul G Fisher, et al.European Journal of Human Genetics : EJHG|October 3, 2013
The MLH1 c.-27C>A and c.85G>T variants are linked to dominantly inherited MLH1 epimutation and are borne on a European ancestral haplotypeChau-To Kwok, Ingrid P Vogelaar, Wendy A van Zelst-Stams, et al.Pageof 1