INVESTIGACIÓN EN ENFERMEDADES RARAS
Hospital San Pedro de Alcántara
Cáceres, EspañaPublikationen in Zusammenarbeit mit Forschern von Hospital San Pedro de Alcántara (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
2020
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Clinical and Molecular Description of 16 Families With Heterozygous IHH Variants
The Journal of clinical endocrinology and metabolism, Vol. 105, Núm. 8