| 000 | 00936 a2200301 4500 | ||
|---|---|---|---|
| 005 | 20250511160828.0 | ||
| 264 | 0 | _c19761029 | |
| 008 | 197610s 0 0 eng d | ||
| 022 | _a0022-2593 | ||
| 024 | 7 |
_a10.1136/jmg.13.4.266 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aCohen, M M | |
| 245 | 0 | 0 |
_aSyndrome designations. _h[electronic resource] |
| 260 |
_bJournal of medical genetics _cAug 1976 |
||
| 300 |
_a266-70 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, U.S. Gov't, Non-P.H.S. | ||
| 650 | 0 | 4 | _aDisease |
| 650 | 0 | 4 | _aEponyms |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Diseases, Inborn |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aSyndrome |
| 650 | 0 | 4 | _aTerminology as Topic |
| 773 | 0 |
_tJournal of medical genetics _gvol. 13 _gno. 4 _gp. 266-70 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1136/jmg.13.4.266 _zAvailable from publisher's website |
| 999 |
_c964905 _d964905 |
||