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1.
Genetics providers' perspectives on the use of digital tools in clinical practice.
Genet Med
; 26(6): 101122, 2024 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-38493336
2.
"The Space Is as Much Yours as It Is Mine": Insights From Health System Leaders About Inclusive Leadership.
Healthc Q
; 27(1): 34-41, 2024 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-38881483
3.
Finding the sweet spot: a qualitative study exploring patients' acceptability of chatbots in genetic service delivery.
Hum Genet
; 142(3): 321-330, 2023 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-36629921
4.
Genetic counselors' response types to prenatal patient deferring or attributing religious/spiritual statements: An exploratory study of US genetic counselors.
J Genet Couns
; 32(1): 197-212, 2023 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-36128752
5.
Genome sequencing among children with medical complexity: What constitutes value from parents' perspective?
J Genet Couns
; 31(2): 523-533, 2022 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-34674352
6.
Who is at risk for compassion fatigue? An investigation of genetic counselor demographics, anxiety, compassion satisfaction, and burnout.
J Genet Couns
; 24(2): 358-70, 2015 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-24781713
7.
Protocol for a Prospective, Observational Cost-effectiveness Analysis of Returning Secondary Findings of Genome Sequencing for Unexplained Suspected Genetic Conditions.
Clin Ther
; 45(8): 702-709, 2023 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-37453830
8.
Comparing genome sequencing technologies to improve rare disease diagnostics: a protocol for the evaluation of a pilot project, Genome-wide Sequencing Ontario.
CMAJ Open
; 10(2): E460-E465, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35609929
9.
Genome sequencing identifies a rare case of moderate Zellweger spectrum disorder caused by a PEX3 defect: Case report and literature review.
Mol Genet Metab Rep
; 25: 100664, 2020 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-33101983
10.
The role of race and ethnicity in views toward and participation in genetic studies and precision medicine research in the United States: A systematic review of qualitative and quantitative studies.
Mol Genet Genomic Med
; 8(2): e1099, 2020 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-31867882
11.
Next generation sequencing for clinical diagnostics: Five year experience of an academic laboratory.
Mol Genet Metab Rep
; 19: 100464, 2019 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-30891420
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