In 19 patients from nine MEN-2A families, high-resolution G-banded chromosome studies have revealed a visible deletion within sub-band 20p12.2, yet no abnormality was observed in a 10th family. A deletion indistinguishable from that in MEN-2A was observed in five patients from three MEN-2B families but not in two other MEN-2B families. We found no abnormality in the entire karyotype of the four MEN-1 patients studied. These findings suggest that the mutation in most MEN-2 patients is a visible deletion in the short arm of chromosome 20.
|Original language||English (US)|
|Number of pages||3|
|Journal||Henry Ford Hospital Medical Journal|
|State||Published - 1984|
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