| 000 | 01459 a2200397 4500 | ||
|---|---|---|---|
| 005 | 20250516003607.0 | ||
| 264 | 0 | _c20110208 | |
| 008 | 201102s 0 0 eng d | ||
| 022 | _a1442-200X | ||
| 024 | 7 |
_a10.1111/j.1442-200X.2010.03181.x _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aErgün, Mehmet A | |
| 245 | 0 | 0 |
_aA case with de novo inv dup del(8p) associated with dextrocardia and corpus callosum agenesis. _h[electronic resource] |
| 260 |
_bPediatrics international : official journal of the Japan Pediatric Society _cOct 2010 |
||
| 300 |
_a845-6 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Letter | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xdiagnosis |
| 650 | 0 | 4 | _aAgenesis of Corpus Callosum |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 | _aChromosome Inversion |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 8 |
| 650 | 0 | 4 | _aConsanguinity |
| 650 | 0 | 4 |
_aCytogenetics _xmethods |
| 650 | 0 | 4 |
_aDextrocardia _xdiagnosis |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 |
_aIntellectual Disability _xdiagnosis |
| 650 | 0 | 4 | _aMicroarray Analysis |
| 650 | 0 | 4 | _aRare Diseases |
| 700 | 1 | _aKula, Serdar | |
| 700 | 1 | _aKaraer, Kadri | |
| 700 | 1 | _aPerçin, E Ferda | |
| 773 | 0 |
_tPediatrics international : official journal of the Japan Pediatric Society _gvol. 52 _gno. 5 _gp. 845-6 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/j.1442-200X.2010.03181.x _zAvailable from publisher's website |
| 999 |
_c20208745 _d20208745 |
||