| 000 | 01486 a2200445 4500 | ||
|---|---|---|---|
| 005 | 20250513094518.0 | ||
| 264 | 0 | _c19961112 | |
| 008 | 199611s 0 0 eng d | ||
| 022 | _a1018-4813 | ||
| 024 | 7 |
_a10.1159/000472177 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aVan de Vosse, E | |
| 245 | 0 | 0 |
_aAn Xp22.1-p22.2 YAC contig encompassing the disease loci for RS, KFSD, CLS, HYP and RP15: refined localization of RS. _h[electronic resource] |
| 260 |
_bEuropean journal of human genetics : EJHG _c1996 |
||
| 300 |
_a101-4 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
| 650 | 0 | 4 | _aChromosome Mapping |
| 650 | 0 | 4 | _aChromosomes, Artificial, Yeast |
| 650 | 0 | 4 |
_aDarier Disease _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aHypophosphatemia, Familial _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 |
_aRetinal Degeneration _xgenetics |
| 650 | 0 | 4 | _aSyndrome |
| 650 | 0 | 4 | _aX Chromosome |
| 700 | 1 | _aBergen, A A | |
| 700 | 1 | _aMeershoek, E J | |
| 700 | 1 | _aOosterwijk, J C | |
| 700 | 1 | _aGregory, S | |
| 700 | 1 | _aBakker, B | |
| 700 | 1 | _aWeissenbach, J | |
| 700 | 1 | _aCoffey, A J | |
| 700 | 1 | _avan Ommen, G J | |
| 700 | 1 | _aDen Dunnen, J T | |
| 773 | 0 |
_tEuropean journal of human genetics : EJHG _gvol. 4 _gno. 2 _gp. 101-4 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1159/000472177 _zAvailable from publisher's website |
| 999 |
_c8741054 _d8741054 |
||