| 000 | 01507 a2200445 4500 | ||
|---|---|---|---|
| 005 | 20250513190833.0 | ||
| 264 | 0 | _c19990902 | |
| 008 | 199909s 0 0 eng d | ||
| 022 | _a0172-0643 | ||
| 024 | 7 |
_a10.1007/s002469900493 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aWeidenbach, M | |
| 245 | 0 | 0 |
_aAcute mitral regurgitation due to chordal rupture in a patient with neonatal Marfan syndrome caused by a deletion in exon 29 of the FBN1 gene. _h[electronic resource] |
| 260 |
_bPediatric cardiology _c |
||
| 300 |
_a382-5 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aAcute Disease |
| 650 | 0 | 4 | _aCause of Death |
| 650 | 0 | 4 | _aChordae Tendineae |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 | _aEchocardiography, Doppler, Color |
| 650 | 0 | 4 |
_aExons _xgenetics |
| 650 | 0 | 4 | _aFatal Outcome |
| 650 | 0 | 4 | _aFibrillin-1 |
| 650 | 0 | 4 | _aFibrillins |
| 650 | 0 | 4 | _aGene Deletion |
| 650 | 0 | 4 |
_aHeart Diseases _xgenetics |
| 650 | 0 | 4 |
_aHeart Failure _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 |
_aMarfan Syndrome _xcomplications |
| 650 | 0 | 4 |
_aMicrofilament Proteins _xgenetics |
| 650 | 0 | 4 |
_aMitral Valve Insufficiency _xdiagnostic imaging |
| 650 | 0 | 4 | _aRupture, Spontaneous |
| 700 | 1 | _aBrenner, R | |
| 700 | 1 | _aRantamäki, T | |
| 700 | 1 | _aRedel, D A | |
| 773 | 0 |
_tPediatric cardiology _gvol. 20 _gno. 5 _gp. 382-5 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s002469900493 _zAvailable from publisher's website |
| 999 |
_c10399448 _d10399448 |
||