Výsledky vyhledávání - Jeffrey N. Weitzel
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Selection of family members for communication of cancer risk and barriers to this communication before and after genetic cancer risk assessment Autor Deborah J. MacDonald, Linda Sarna, Gwen van Servellen, Roshan Bastani, Joyce Newman Giger, Jeffrey N. Weitzel
Vydáno 2007Artigo -
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Li-Fraumeni syndrome: not a straightforward diagnosis anymore—the interpretation of pathogenic variants of low allele frequency and the differences between germline PVs, mosaicism,... Autor Felipe Batalini, Ellie G. Peacock, Lindsey Stobie, Alison Robertson, Judy E. Garber, Jeffrey N. Weitzel, Nadine Tung
Vydáno 2019Revisão -
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Quality of Cancer Family History and Referral for Genetic Counseling and Testing Among Oncology Practices: A Pilot Test of Quality Measures As Part of the American Society of Clini... Autor Marie Wood, Pamela Kadlubek, Trang Pham, Dana S. Wollins, Karen H. Lu, Jeffrey N. Weitzel, Michael N. Neuss, Kevin S. Hughes
Vydáno 2014Artigo -
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Personalized cancer genetics training for personalized medicine: Improving community-based healthcare through a genetically literate workforce Autor Kathleen R. Blazer, Deborah J. MacDonald, Julie O. Culver, Carin R. Huizenga, Robert J. Morgan, Gwen Uman, Jeffrey N. Weitzel
Vydáno 2011Artigo -
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Participation of low-income women in genetic cancer risk assessment and BRCA 1/2 testing: the experience of a safety-net institution Autor Ian K. Komenaka, Jesse Nodora, Lisa Madlensky, Lisa M. Winton, M Heberer, Richard B. Schwab, Jeffrey N. Weitzel, Marı́a Elena Martı́nez
Vydáno 2015Artigo -
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Reflex Immunohistochemistry and Microsatellite Instability Testing of Colorectal Tumors for Lynch Syndrome Among US Cancer Programs and Follow-Up of Abnormal Results Autor Laura Curr Beamer, Marcia L. Grant, Carin R. Espenschied, Kathleen R. Blazer, Heather L. Hampel, Jeffrey N. Weitzel, Deborah J. MacDonald
Vydáno 2012Artigo -
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Vyhledávací nástroje:
Související témata
Medicine
Cancer
Biology
Genetics
Internal medicine
Gene
Oncology
Breast cancer
Mutation
Germline mutation
Genetic testing
Ovarian cancer
Gynecology
Genotype
Germline
Population
BRCA mutation
Environmental health
Genetic counseling
Single-nucleotide polymorphism
Family history
Bioinformatics
Family medicine
Cancer research
Colorectal cancer
Computer science
Confidence interval
Allele
DNA mismatch repair
Sociology