000 01077 a2200337 4500
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