Frank W. Crowe
In 1956 Crowe et al. recognised the autosomal dominant heredity of neurofibromatosis and the use of 6 or more café au lait spots to diagnose the condition. In 1964 Crowe published work on the use of axillary freckling in its diagnosis, which is now referred to as the Crowe sign.
- Frank W. Crowe, William J. Schull, James V. Neel. Multiple Neurofibromatosis. Charles C Thomas, Publisher, 301–327 E. Lawrence Ave., Springfield, Ill., 1956.
- Crowe FW (December 1964). "Axillary Freckling as a Diagnostic Aid in Neurofibromatosis". Ann. Intern. Med. 61: 1142–3. doi:10.7326/0003-4819-61-6-1142. PMID 14233837.
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