| 000 | 00846 a2200253 4500 | ||
|---|---|---|---|
| 005 | 20250510210718.0 | ||
| 264 | 0 | _c19770630 | |
| 008 | 197706s 0 0 eng d | ||
| 022 | _a0140-6736 | ||
| 024 | 7 |
_a10.1016/s0140-6736(77)92300-5 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aEdwards, J H | |
| 245 | 0 | 0 |
_aIncidence of hereditary disease in man. _h[electronic resource] |
| 260 |
_bLancet (London, England) _cMay 1977 |
||
| 300 |
_a1003-4 p. _bdigital |
||
| 500 | _aPublication Type: Letter | ||
| 650 | 0 | 4 | _aChromosome Aberrations |
| 650 | 0 | 4 | _aGenes, Dominant |
| 650 | 0 | 4 |
_aGenetic Diseases, Inborn _xepidemiology |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMutation |
| 773 | 0 |
_tLancet (London, England) _gvol. 1 _gno. 8019 _gp. 1003-4 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/s0140-6736(77)92300-5 _zAvailable from publisher's website |
| 999 |
_c65684 _d65684 |
||