000 | 01077 a2200337 4500 | ||
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005 | 20250516093038.0 | ||
264 | 0 | _c20120719 | |
008 | 201207s 0 0 eng d | ||
022 | _a1015-8146 | ||
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aTug, E | |
245 | 0 | 0 |
_aThrombophilia gene mutations in oculoauriculovertebral spectrum. _h[electronic resource] |
260 |
_bGenetic counseling (Geneva, Switzerland) _c2012 |
||
300 |
_a65-72 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article | ||
650 | 0 | 4 |
_aFacial Asymmetry _xgenetics |
650 | 0 | 4 |
_aFactor V _xgenetics |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 |
_aGoldenhar Syndrome _xgenetics |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aInfant |
650 | 0 | 4 | _aInfant, Newborn |
650 | 0 | 4 | _aMale |
650 | 0 | 4 |
_aMethylenetetrahydrofolate Reductase (NADPH2) _xgenetics |
650 | 0 | 4 | _aMutation |
650 | 0 | 4 |
_aProthrombin _xgenetics |
650 | 0 | 4 | _aSeverity of Illness Index |
700 | 1 | _aAtasoy, H I | |
700 | 1 | _aKoybasi Sanal, S | |
773 | 0 |
_tGenetic counseling (Geneva, Switzerland) _gvol. 23 _gno. 1 _gp. 65-72 |
|
999 |
_c21796956 _d21796956 |