UNIOVI-PEDIATRIA
OVIPED
Istituto Superiore di Sanità
Roma, ItaliaIstituto Superiore di Sanità-ko ikertzaileekin lankidetzan egindako argitalpenak (1)
2021
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Compound heterozygosity for PTPN11 variants in a subject with Noonan syndrome provides insights into the mechanism of SHP2-related disorders
Clinical Genetics, Vol. 99, Núm. 3, pp. 457-461