| 000 | 01611 a2200433 4500 | ||
|---|---|---|---|
| 005 | 20250514161056.0 | ||
| 264 | 0 | _c20040412 | |
| 008 | 200404s 0 0 eng d | ||
| 022 | _a0340-6717 | ||
| 024 | 7 |
_a10.1007/s00439-003-1029-y _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aBallif, Blake C | |
| 245 | 0 | 0 |
_aTranslocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements. _h[electronic resource] |
| 260 |
_bHuman genetics _cJan 2004 |
||
| 300 |
_a198-206 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. | ||
| 650 | 0 | 4 | _aChromosome Aberrations |
| 650 | 0 | 4 | _aChromosome Banding |
| 650 | 0 | 4 | _aChromosome Disorders |
| 650 | 0 | 4 | _aChromosome Mapping |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 1 _xgenetics |
| 650 | 0 | 4 |
_aCytogenetic Analysis _xmethods |
| 650 | 0 | 4 |
_aDNA _xgenetics |
| 650 | 0 | 4 | _aDNA Probes |
| 650 | 0 | 4 |
_aDNA Replication _xgenetics |
| 650 | 0 | 4 | _aGene Deletion |
| 650 | 0 | 4 | _aGene Rearrangement |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIn Situ Hybridization, Fluorescence |
| 650 | 0 | 4 |
_aMonosomy _xgenetics |
| 650 | 0 | 4 |
_aRepetitive Sequences, Nucleic Acid _xgenetics |
| 650 | 0 | 4 |
_aTelomere _xgenetics |
| 650 | 0 | 4 | _aTranslocation, Genetic |
| 700 | 1 | _aWakui, Keiko | |
| 700 | 1 | _aGajecka, Marzena | |
| 700 | 1 | _aShaffer, Lisa G | |
| 773 | 0 |
_tHuman genetics _gvol. 114 _gno. 2 _gp. 198-206 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s00439-003-1029-y _zAvailable from publisher's website |
| 999 |
_c14320921 _d14320921 |
||