| 000 | 01797 a2200529 4500 | ||
|---|---|---|---|
| 005 | 20250515043041.0 | ||
| 264 | 0 | _c20070329 | |
| 008 | 200703s 0 0 eng d | ||
| 022 | _a1018-4813 | ||
| 024 | 7 |
_a10.1038/sj.ejhg.5201718 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aBrenk, Christian H | |
| 245 | 0 | 0 |
_aTowards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation. _h[electronic resource] |
| 260 |
_bEuropean journal of human genetics : EJHG _cJan 2007 |
||
| 300 |
_a35-44 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Breakage |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 | _aChromosome Mapping |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 18 |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 20 |
| 650 | 0 | 4 | _aFace |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIn Situ Hybridization, Fluorescence |
| 650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
| 650 | 0 | 4 | _aKaryotyping |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aSyndrome |
| 650 | 0 | 4 | _aTranslocation, Genetic |
| 700 | 1 | _aPrott, Eva-Christina | |
| 700 | 1 | _aTrost, Detlef | |
| 700 | 1 | _aHoischen, Alexander | |
| 700 | 1 | _aWalldorf, Constanze | |
| 700 | 1 | _aRadlwimmer, Bernhard | |
| 700 | 1 | _aWieczorek, Dagmar | |
| 700 | 1 | _aPropping, Peter | |
| 700 | 1 | _aGillessen-Kaesbach, Gabriele | |
| 700 | 1 | _aWeber, Ruthild G | |
| 700 | 1 | _aEngels, Hartmut | |
| 773 | 0 |
_tEuropean journal of human genetics : EJHG _gvol. 15 _gno. 1 _gp. 35-44 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1038/sj.ejhg.5201718 _zAvailable from publisher's website |
| 999 |
_c16601111 _d16601111 |
||