Bertola, Débora Romeo
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Monogenic diseases with low bone mineral density: clinical and genetic evaluation...
Genetic-Clinical study of skeletal dysplasias, with a focus on osteochondrodysplasias...
Study of PTPN11 and KRAS genes in patients with Noonan and Noonan-like syndrome...
Genetic determinants in Noonan syndrome and in Noonan-like syndromes: clinical and...
Genetic basis of vertebral segmentation defects: genetic and clinical study focused...
Characterization of the nutritional status of patients with Noonan syndrome and Noonan-like...
Genetic study of patients with Rothmund-Thomson syndrome
Genetic and clinical study of patients with progerioid syndromes
Clinical and molecular study of patients with Noonan syndrome and Noonan-related...
Genomic study of individuals with congenital limb deficiency
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