INVESTIGACIÓN EN ENFERMEDADES RARAS
Universitat Pompeu Fabra
Barcelona, EspañaPublications en collaboration avec des chercheurs de Universitat Pompeu Fabra (2)
2022
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Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants
Genetics in Medicine, Vol. 24, Núm. 11, pp. 2351-2366
2016
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Clinical and molecular analyses of Beckwith–Wiedemann syndrome: Comparison between spontaneous conception and assisted reproduction techniques
American Journal of Medical Genetics, Part A, Vol. 170, Núm. 10, pp. 2740-2749