Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mollie L. Hutton"'
Autor:
Jennifer K. Litton, Kenneth Offit, Christine Laronga, Matthew B. Yurgelun, Leigha Senter-Jamieson, Kristen M. Shannon, Ahmed Elkhanany, Beth Y. Karlan, Seema A. Khan, Susan M. Domchek, Kari B. Wisinski, Patricia I. Dickson, Gwen Reiser, Holly J. Pederson, Catherine Klein, Barbara S. Norquist, Mary B. Daly, Allison W. Kurian, Wendy Kohlmann, Carolyn S. Menendez, Jeffrey N. Weitzel, Mary A. Dwyer, Mollie L. Hutton, Susan Darlow, Kala Visvanathan, Sofia D. Merajver, Rebecca Shatsky, Myra J. Wick, Michael Goggins, Saundra S. Buys, Michael Berry, Susan Hatters Friedman, Julie S. Mak, Tuya Pal
Publikováno v:
Journal of the National Comprehensive Cancer Network. 19:77-102
The NCCN Guidelines for Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic focus primarily on assessment of pathogenic or likely pathogenic variants associated with increased risk of breast, ovarian, and pancreatic cancer and reco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9b57ad3ed257825a4301e48dcd971c4
https://doi.org/10.6004/jnccn.2021.0001
https://doi.org/10.6004/jnccn.2021.0001
Autor:
Mollie L. Hutton, Mary A. Dwyer, Catherine Klein, Robert Pilarski, Kala Visvanathan, Michael Goggins, Susan Darlow, Myra J. Wick, Carolyn S. Menendez, Jennifer K. Litton, Kenneth Offit, Gwen Reiser, Seema A. Khan, Holly J. Pederson, Matthew B. Yurgelun, Patricia I. Dickson, Mary B. Daly, Allison W. Kurian, Christine Laronga, Sofia D. Merajver, Kari B. Wisinski, Barbara S. Norquist, Michael Berry, Saundra S. Buys, Susan Hatters Friedman, Wendy Kohlmann, Jeffrey N. Weitzel, Julie S. Mak, Ahmed Elkhanany, Judy Garber, Kristen M. Shannon, Susan M. Domchek, Tuya Pal
Publikováno v:
Journal of the National Comprehensive Cancer Network. 18:380-391
The NCCN Guidelines for Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic provide recommendations for genetic testing and counseling for hereditary cancer syndromes, and risk management recommendations for patients who are diagno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b39e974208603592707867505730eb8e
https://doi.org/10.6004/jnccn.2020.0017
https://doi.org/10.6004/jnccn.2020.0017
Autor:
J. Brian Szender, Jasmine Kaur, June Mikkelson, Mollie L. Hutton, Katherine Clayback, Cara Dresbold, Kunle Odunsi
Publikováno v:
International journal of gynecological cancer : official journal of the International Gynecological Cancer Society. 28(1)
ObjectiveThe aim of this study was to evaluate the ability of patients at risk of hereditary breast and ovarian cancer (HBOC) syndrome to select the extent of genetic testing personally preferred and the impact of demographic factors on the breadth o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4778efffc91d952b15f4b0e7978ffaa6
https://pubmed.ncbi.nlm.nih.gov/28930807
https://pubmed.ncbi.nlm.nih.gov/28930807