000 01513 a2200457 4500
005 20250517023557.0
264 0 _c20160225
008 201602s 0 0 eng d
022 _a1538-7836
024 7 _a10.1111/jth.12916
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aCasini, A
245 0 0 _aDysfibrinogenemia: from molecular anomalies to clinical manifestations and management.
_h[electronic resource]
260 _bJournal of thrombosis and haemostasis : JTH
_cJun 2015
300 _a909-19 p.
_bdigital
500 _aPublication Type: Journal Article; Review
650 0 4 _aAfibrinogenemia
_xblood
650 0 4 _aAnimals
650 0 4 _aBlood Coagulation
_xgenetics
650 0 4 _aBlood Coagulation Tests
650 0 4 _aDNA Mutational Analysis
650 0 4 _aFemale
650 0 4 _aFibrinogens, Abnormal
_xgenetics
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMolecular Diagnostic Techniques
650 0 4 _aMutation
650 0 4 _aPhenotype
650 0 4 _aPredictive Value of Tests
650 0 4 _aPregnancy
650 0 4 _aPregnancy Complications, Hematologic
_xblood
650 0 4 _aPrognosis
650 0 4 _aRisk Factors
650 0 4 _aThrombosis
_xblood
700 1 _aNeerman-Arbez, M
700 1 _aAriƫns, R A
700 1 _ade Moerloose, P
773 0 _tJournal of thrombosis and haemostasis : JTH
_gvol. 13
_gno. 6
_gp. 909-19
856 4 0 _uhttps://doi.org/10.1111/jth.12916
_zAvailable from publisher's website
999 _c24749651
_d24749651