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Science 27 January 1978: Vol. 199. no. 4327, pp. 429 - 431 DOI: 10.1126/science.619463
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Articles
Science, Vol 199, Issue 4327, 429-431
Copyright © 1978 by American Association for the Advancement of Science
Inherited medullary thyroid carcinoma: a final monoclonal mutation in one of multiple clones of susceptible cells
SB Baylin,
SH Hsu,
DS Gann,
RC Smallridge,
and
SA Wells Jr
Inherited medullary thyroid carcinomas contain one form of glucose-6-phosphate dehydrogenase (G6PD) in black female patients who are mosaic in normal tissues for G6PD types A and B. The same individual may have several tumors each containing either G6PD A or G6PD B. The data suggest that the inherited defect is an initial mutation producing multiple clones of defective cells; each tumor then arises as a final mutation in one clone of these cells.
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