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Home > Our Research Activities > List Of Publications > Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann-Steiner and Rubinstein-Taybi syndromes

Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann-Steiner and Rubinstein-Taybi syndromes

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Variants of SOS2 are a rare cause of Noonan syndrome with particular predisposition for lymphatic complications

Chondrodysplasia and growth failure in children after early hematopoietic stem cell transplantation for non-oncologic disorders

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