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1.
NCCN Guidelines® Insights: Breast Cancer Screening and Diagnosis, Version 1.2023.
J Natl Compr Canc Netw
; 21(9): 900-909, 2023 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-37673117
2.
Diversity training experiences and factors associated with implicit racial bias among recent genetic counselor graduates of accredited programs in the United States and Canada.
J Genet Couns
; 31(3): 792-802, 2022 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-35040227
3.
Factors affecting breast cancer patients' need for genetic risk information: From information insufficiency to information need.
J Genet Couns
; 28(3): 543-557, 2019 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-30675956
4.
Information Topics of Greatest Interest for Return of Genome Sequencing Results among Women Diagnosed with Breast Cancer at a Young Age.
J Genet Couns
; 26(3): 511-521, 2017 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-27542972
5.
Psychosocial and Clinical Factors Associated with Family Communication of Cancer Genetic Test Results among Women Diagnosed with Breast Cancer at a Young Age.
J Genet Couns
; 26(1): 173-181, 2017 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-27422778
6.
MonoSeq Variant Caller Reveals Novel Mononucleotide Run Indel Mutations in Tumors with Defective DNA Mismatch Repair.
Hum Mutat
; 37(10): 1004-12, 2016 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-27346418
7.
Previously unreported somatic variants in two patients with pleuropulmonary blastoma with metastatic brain recurrence.
Pediatr Blood Cancer
; 68(5): e28825, 2021 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-33258270
8.
DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome.
Nature
; 456(7218): 66-72, 2008 Nov 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-18987736
9.
Pediatric precision oncology: "better three hours too soon than a minute too late".
Front Oncol
; 13: 1279953, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-38023209
10.
TERC and TERT gene mutations in patients with bone marrow failure and the significance of telomere length measurements.
Blood
; 113(2): 309-16, 2009 Jan 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-18931339
11.
Identification of a novel TP53 cancer susceptibility mutation through whole-genome sequencing of a patient with therapy-related AML.
JAMA
; 305(15): 1568-76, 2011 Apr 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-21505135
12.
Rare BRIP1 Missense Alleles Confer Risk for Ovarian and Breast Cancer.
Cancer Res
; 80(4): 857-867, 2020 02 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-31822495
13.
Telomerase reverse transcriptase haploinsufficiency and telomere length in individuals with 5p- syndrome.
Aging Cell
; 6(5): 689-97, 2007 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-17875000
14.
Preferences for learning different types of genome sequencing results among young breast cancer patients: Role of psychological and clinical factors.
Transl Behav Med
; 8(1): 71-79, 2018 01 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-29385583
15.
Managing breast cancer in younger women: challenges and solutions.
Breast Cancer (Dove Med Press)
; 8: 1-12, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-26730210
16.
How, who, and when: preferences for delivery of genome sequencing results among women diagnosed with breast cancer at a young age.
Mol Genet Genomic Med
; 4(6): 684-695, 2016 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-27896289
17.
Lymphovascular space invasion and lack of downstaging after neoadjuvant chemotherapy are strong predictors of adverse outcome in young women with locally advanced breast cancer.
Cancer Med
; 5(2): 230-8, 2016 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-26687192
18.
Evaluation of the family history collection process and the accuracy of cancer reporting among a series of women with endometrial cancer.
Clin Cancer Res
; 8(6): 1849-56, 2002 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-12060627
19.
Sustained Complete Response to Palbociclib in a Refractory Pediatric Sarcoma With BCOR-CCNB3 Fusion and Germline CDKN2B Variant.
JCO Precis Oncol
; 42020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32923894
20.
Temporal order of RNase IIIb and loss-of-function mutations during development determines phenotype in pleuropulmonary blastoma / DICER1 syndrome: a unique variant of the two-hit tumor suppression model.
F1000Res
; 4: 214, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26925222