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1.
Expectations, needs and mid-term outcomes in people accessing to secondary findings from ES: 1st French mixed study (FIND Study).
Eur J Hum Genet
; 2024 May 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-38802530
2.
Access to social services for undiagnosed rare disease patients in France: A pilot study.
Eur J Med Genet
; 65(5): 104494, 2022 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-35385796
3.
Exome sequencing in clinical settings: preferences and experiences of parents of children with rare diseases (SEQUAPRE study).
Eur J Hum Genet
; 27(5): 701-710, 2019 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-30710147
4.
Secondary actionable findings identified by exome sequencing: expected impact on the organisation of care from the study of 700 consecutive tests.
Eur J Hum Genet
; 27(8): 1197-1214, 2019 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-31019283
5.
Preference heterogeneity with respect to whole genome sequencing. A discrete choice experiment among parents of children with rare genetic diseases.
Soc Sci Med
; 214: 125-132, 2018 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-30179780
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