| 000 | 01447 a2200409 4500 | ||
|---|---|---|---|
| 005 | 20250513130416.0 | ||
| 264 | 0 | _c19971125 | |
| 008 | 199711s 0 0 eng d | ||
| 022 | _a0301-0171 | ||
| 024 | 7 |
_a10.1159/000134628 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aHill, A | |
| 245 | 0 | 0 |
_aAssignment of fragile site 8E (FRA8E) to human chromosome band 8q24.11 adjacent to the hereditary multiple exostoses 1 gene and two overlapping Langer-Giedion syndrome deletion endpoints. _h[electronic resource] |
| 260 |
_bCytogenetics and cell genetics _c1997 |
||
| 300 |
_a56-7 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. | ||
| 650 | 0 | 4 | _aCell Line |
| 650 | 0 | 4 | _aChromosome Banding |
| 650 | 0 | 4 | _aChromosome Fragile Sites |
| 650 | 0 | 4 | _aChromosome Fragility |
| 650 | 0 | 4 | _aChromosome Mapping |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 8 |
| 650 | 0 | 4 | _aCosmids |
| 650 | 0 | 4 |
_aExostoses _xgenetics |
| 650 | 0 | 4 | _aGene Deletion |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIn Situ Hybridization, Fluorescence |
| 650 | 0 | 4 |
_aLanger-Giedion Syndrome _xgenetics |
| 650 | 0 | 4 |
_aLymphocytes _xcytology |
| 700 | 1 | _aHarada, Y | |
| 700 | 1 | _aTakahashi, E | |
| 700 | 1 | _aHou, J | |
| 700 | 1 | _aWagner, M J | |
| 700 | 1 | _aWells, D E | |
| 773 | 0 |
_tCytogenetics and cell genetics _gvol. 78 _gno. 1 _gp. 56-7 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1159/000134628 _zAvailable from publisher's website |
| 999 |
_c9316840 _d9316840 |
||