Detalles de la búsqueda
1.
"Not pathogenic until proven otherwise": perspectives of UK clinical genomics professionals toward secondary findings in context of a Genomic Medicine Multidisciplinary Team and the 100,000 Genomes Project.
Genet Med
; 20(3): 320-328, 2018 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-29261176
2.
Expect the unexpected: screening for secondary findings in clinical genomics research.
Br Med Bull
; 122(1): 109-122, 2017 06 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-28398474
3.
Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.
Genet Med
; 19(3): 283-293, 2017 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-27584911
4.
Gyrodactylus laevisoides n. sp. (Monogenea: Gyrodactylidae) infecting northern redbelly dace Phoxinus eos Cope (Cyprinidae) from Nova Scotia, Canada.
Syst Parasitol
; 86(3): 285-91, 2013 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-24163028
5.
A Rare Hemoglobin Variant (ß51Proâ ââ His) Causing Misleading Measurements of Hemoglobin A1c.
J Endocr Soc
; 6(4): bvab186, 2022 Apr 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-35237735
6.
Rare Disease Education Outside of the Classroom and Clinic: Evaluation of the RARE Compassion Program for Undergraduate Medical Students.
Genes (Basel)
; 13(10)2022 Sep 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-36292592
7.
Revisiting Risk and Benefit in Early Oncology Trials in the Era of Precision Medicine: A Systematic Review and Meta-Analysis of Phase I Trials of Targeted Single-Agent Anticancer Therapies.
JCO Precis Oncol
; 5: 17-26, 2021 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-34994588
8.
Secondary findings in inherited heart conditions: a genotype-first feasibility study to assess phenotype, behavioural and psychosocial outcomes.
Eur J Hum Genet
; 28(11): 1486-1496, 2020 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-32686758
9.
Equity implications of patient-initiated recontact and follow-up in clinical genetics.
Eur J Hum Genet
; 31(5): 495-496, 2023 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-36959498
10.
Views of rare disease participants in a UK whole-genome sequencing study towards secondary findings: a qualitative study.
Eur J Hum Genet
; 26(5): 652-659, 2018 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-29440777
11.
Insights from early experience of a Rare Disease Genomic Medicine Multidisciplinary Team: a qualitative study.
Eur J Hum Genet
; 25(6): 680-686, 2017 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-28327571
12.
Complete mitochondrial genomes for Icelus spatula, Aspidophoroides olrikii and Leptoclinus maculatus: pan-Arctic marine fishes from Canadian waters.
Mitochondrial DNA A DNA Mapp Seq Anal
; 27(4): 2982-3, 2016 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-26122337
13.
Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutations.
JAMA Ophthalmol
; 132(12): 1393-9, 2014 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-25124931
Resultados
1 -
13
de 13
1
Próxima >
>>