Idézéskapcsolat

Oriola J et al. Clinical spectrum of MEN2A in a large family caused by the infrequent RET mutation Cys609Phe. (2013) CLINICAL GENETICS 0009-9163 1399-0004 83 4 384-387

Közlemény:
Igaz P et al. Occurrence of pheochromocytoma in a MEN2A family with codon 609 mutation of the RET proto-oncogene. (2002) JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM 0021-972X 1945-7197 87 6 p. 2994
Idéző közlemény:
Oriola J et al. Clinical spectrum of MEN2A in a large family caused by the infrequent RET mutation Cys609Phe. (2013) CLINICAL GENETICS 0009-9163 1399-0004 83 4 384-387
Független: Igen
2021-05-12 22:57