Detalhe da pesquisa
1.
Genetic counselors' and community clinicians' implementation and perceived barriers to informed consent during pre-test counseling for hereditary cancer risk.
J Genet Couns
; 2024 Mar 13.
Artigo
Inglês
| MEDLINE | ID: mdl-38480478
2.
Clinical and laboratory genetic counselor attitudes on the reporting of variants of uncertain significance for multigene cancer panels.
J Genet Couns
; 32(3): 706-716, 2023 06.
Artigo
Inglês
| MEDLINE | ID: mdl-36747331
3.
Anaplastic Astrocytoma in a Child With Coffin-Siris Syndrome and a Germline SMARCE1 Mutation: A Case Report.
J Pediatr Hematol Oncol
; 42(3): e177-e180, 2020 04.
Artigo
Inglês
| MEDLINE | ID: mdl-30499906
4.
Speaking genomics to parents offered germline testing for cancer predisposition: Use of a 2-visit consent model.
Cancer
; 125(14): 2455-2464, 2019 07 15.
Artigo
Inglês
| MEDLINE | ID: mdl-30901077
5.
Integrating next-generation sequencing into pediatric oncology practice: An assessment of physician confidence and understanding of clinical genomics.
Cancer
; 123(12): 2352-2359, 2017 Jun 15.
Artigo
Inglês
| MEDLINE | ID: mdl-28192596
6.
Calcaneonavicular Coalition Resection With Pes Planovalgus Reconstruction.
J Foot Ankle Surg
; 55(3): 578-82, 2016.
Artigo
Inglês
| MEDLINE | ID: mdl-26964697
7.
Genomes for Kids: The Scope of Pathogenic Mutations in Pediatric Cancer Revealed by Comprehensive DNA and RNA Sequencing.
Cancer Discov
; 11(12): 3008-3027, 2021 12 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34301788
8.
From uncertainty to pathogenicity: clinical and functional interrogation of a rare TP53 in-frame deletion.
Cold Spring Harb Mol Case Stud
; 5(4)2019 08.
Artigo
Inglês
| MEDLINE | ID: mdl-30886117