학술논문
Multiple molecular diagnoses in the field of intellectual disability and congenital anomalies: 3.5% of all positive cases
Document Type
Article
Author
Racine, C.; Sorlin, A.; Nambot, S.; Delanne, J.; Garde, A.; Colin, E.; Moutton, S.; Thevenon, J.; Jean-Marçais, N.; Faivre, L.; Thauvin-Robinet, C.; Denommé-Pichon, A.-S.; Engel, C.; Tran Mau-Them, F.; Bruel, A.-L.; Vitobello, A.; Safraou, H.; Bourgeois, V.; Poe, C.; Chevarin, M.; Couturier, V.; Garret, P.; Philippe, C.; Duffourd, Y.; Willems, M.; Geneviève, D.; Pinson, L.; Perrin, L.; Laffargue, F.; Lespinasse, J.; Lacaze, E.; Molin, A.; Gerard, M.; Lambert, L.; Benigni, C.; Patat, O.
Source
In: Journal of Medical Genetics . (Journal of Medical Genetics, 16 August 2023, 61(1):36-46)
Subject
Language
English
ISSN
14686244
00222593
00222593