Scarcity of available information resources for patients and clinicians after a diagnosis of ultra-rare diseases: retrospective on a cohort of 626 individuals with congenital abnormalities and/or intellectual disability - Université de Rennes Accéder directement au contenu
Article Dans Une Revue European Journal of Human Genetics Année : 2022

Scarcity of available information resources for patients and clinicians after a diagnosis of ultra-rare diseases: retrospective on a cohort of 626 individuals with congenital abnormalities and/or intellectual disability

Résumé

Meeting Abstract P23.046.B
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Dates et versions

hal-03687603 , version 1 (03-06-2022)

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  • HAL Id : hal-03687603 , version 1

Citer

Paul Rollier, Sandrine de Montgolfier, Christèle Dubourg, Wilfrid Carre, Véronique David, et al.. Scarcity of available information resources for patients and clinicians after a diagnosis of ultra-rare diseases: retrospective on a cohort of 626 individuals with congenital abnormalities and/or intellectual disability. European Journal of Human Genetics, 2022, 30 (SUPPL 1), pp.583-583. ⟨hal-03687603⟩
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