Recurrent pregnancy loss and its relation to combined parental thrombophilic gene mutations

Genetic Testing and Molecular Biomarkers

Volumn 16, Issue 4, 2012, Pages 279-286

  Ozdemir, Oztürk ^a,b   Yenicesu, Gonca Imir ^b   Silan, Fatma ^a   Köksal, Binnur ^b   Atik, Sinem ^a   Ozen, Filiz ^b   Göl, Mert ^a   Cetin, Ali ^b  

^a ÇANAKKALE ONSEKIZ MART UNIVERSITY   (Turkey)

^b CUMHURIYET UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA;

ADULT; ANTIPHOSPHOLIPID SYNDROME; ARTICLE; DISEASE ASSOCIATION; ETHNIC GROUP; FATHER; FEMALE; GENE MUTATION; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MOTHER; PARENT; PREGNANCY COMPLICATION; REAL TIME POLYMERASE CHAIN REACTION; RECURRENT ABORTION; RECURRENT DISEASE; RECURRENT PREGNANCY LOSS; THROMBOPHILIA; TURKEY (REPUBLIC);

ABORTION, HABITUAL; ADOLESCENT; ADULT; ALLELES; APOLIPOPROTEIN E2; APOLIPOPROTEIN E4; FACTOR V; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HETEROZYGOTE; HOMOZYGOTE; HUMANS; MALE; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); MUTATION; PARENTS; PLASMINOGEN ACTIVATOR INHIBITOR 1; PREGNANCY; PREGNANCY COMPLICATIONS, HEMATOLOGIC; THROMBOPHILIA; TURKEY; YOUNG ADULT;

EID: 84860197151     PISSN: 19450265     EISSN: 19450257     Source Type: Journal    
DOI: 10.1089/gtmb.2011.0191     Document Type: Article

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