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Autor:
P. Groth, Friedhelm Raue, Karin Frank-Raue, Marlene Reuter, Michael M. Ritter, Wolfgang Höppner, M. Grußendorf, B. Saller, Ilona Berndt
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 83:770-774
One hundred and eighty-one families with multiple endocrine neoplasia type 2A (MEN-2A) or familial medullary thyroid carcinoma (FMTC) have been investigated for mutations in the ret protooncogene in Germany. In 8 families with FMTC or MEN-2A, no muta