| 000 | 01869 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250515155129.0 | ||
| 264 | 0 | _c20091008 | |
| 008 | 200910s 0 0 eng d | ||
| 022 | _a1476-5438 | ||
| 024 | 7 |
_a10.1038/ejhg.2008.269 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aZhang, Litu | |
| 245 | 0 | 0 |
_aCharacterization of a t(5;8)(q31;q21) translocation in a patient with mental retardation and congenital heart disease: implications for involvement of RUNX1T1 in human brain and heart development. _h[electronic resource] |
| 260 |
_bEuropean journal of human genetics : EJHG _cAug 2009 |
||
| 300 |
_a1010-8 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aAnimals |
| 650 | 0 | 4 |
_aBrain _xembryology |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 5 |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 8 |
| 650 | 0 | 4 |
_aHeart _xembryology |
| 650 | 0 | 4 |
_aHeart Defects, Congenital _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMice |
| 650 | 0 | 4 |
_aMyocardium _xmetabolism |
| 650 | 0 | 4 |
_aProto-Oncogene Proteins _xgenetics |
| 650 | 0 | 4 | _aRUNX1 Translocation Partner 1 Protein |
| 650 | 0 | 4 |
_aTranscription Factors _xgenetics |
| 650 | 0 | 4 | _aTranslocation, Genetic |
| 700 | 1 | _aTümer, Zeynep | |
| 700 | 1 | _aMøllgård, Kjeld | |
| 700 | 1 | _aBarbi, Gotthold | |
| 700 | 1 | _aRossier, Eva | |
| 700 | 1 | _aBendsen, Eske | |
| 700 | 1 | _aMøller, Rikke Steensbjerre | |
| 700 | 1 | _aUllmann, Reinhard | |
| 700 | 1 | _aHe, Jian | |
| 700 | 1 | _aPapadopoulos, Nickolas | |
| 700 | 1 | _aTommerup, Niels | |
| 700 | 1 | _aLarsen, Lars Allan | |
| 773 | 0 |
_tEuropean journal of human genetics : EJHG _gvol. 17 _gno. 8 _gp. 1010-8 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1038/ejhg.2008.269 _zAvailable from publisher's website |
| 999 |
_c18619285 _d18619285 |
||