Melkersson‐Rosenthal syndrome and de novo autosomal t(9;21)(p11;p11) translocation

Abstract excerpt

In this report we describe a 26-year-old female with the typical clinical symptoms and signs of Melkersson-Rosenthal syndrome, an autosomal dominant with variable expression, and a de novo t(9;21)(p11;p11), and suggest that the "Melkersson-Rosenthal gene" is located at 9p11.

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