Copyright © Philip M. Parker, INSEAD. Terms of Use.
| Domain | Definition |
Health | Hereditary disorder transmitted by an autosomal dominant gene and characterized by multiple exostoses (multiple osteochondromas) near the ends of long bones. The genetic abnormality results in a defect in the osteoclastic activity at the metaphyseal ends of the bone during the remodeling process in childhood or early adolescence. The metaphyses develop benign, bony outgrowths often capped by cartilage. A small number undergo neoplastic transformation. (references) |
Source: compiled by the editor from various references; see credits. | |
Hexadecimal (or equivalents, 770AD-1900s) (references)45 58 4F 53 54 4F 53 45 53 2C 4D 55 4C 54 49 50 4C 45 48 45 52 45 44 49 54 41 52 59 |
| Leonardo da Vinci (1452-1519; backwards) (references)
|
Binary Code (1918-1938, probably earlier) (references)01000101 01011000 01001111 01010011 01010100 01001111 01010011 01000101 01010011 00101100 00100000 01001101 01010101 01001100 01010100 01001001 01010000 01001100 01000101 00100000 01001000 01000101 01010010 01000101 01000100 01001001 01010100 01000001 01010010 01011001 |
HTML Code (1990) (references)E X O S T O S E S ,   M U L T I P L E   H E R E D I T A R Y |
ISO 10646 (1991-1993) (references)0045 0058 004F 0053 0054 004F 0053 0045 0053 002C 004D 0055 004C 0054 0049 0050 004C 0045 0048 0045 0052 0045 0044 0049 0054 0041 0052 0059 |
Encryption (beginner's substitution cypher): (references)3958495354495339531424755465443504639242395239384354355259 |
| 1. Orthography 2. Bibliography |
Copyright © Philip M. Parker, INSEAD. Terms of Use.
