AXILLARY ARTERY THROMBOSIS IN A NEWBORN HOMOZYGOUS FOR METHYLENETETRAHYDROFOLATE REDUCTASE (A1298C) MUTATION AND HETEROZYGOUS FOR FACTOR V LEIDEN (G506A) MUTATION.

Dilli, D; Fettah, N; Çinar, H G; Özyazici, E; Dursun, A; Zenciroglu, A; Okumus, N

Dilli, D; Fettah, N; Çinar, H G; Özyazici, E; Dursun, A; Zenciroglu, A; Okumus, N.

Genet Couns ; 27(1): 87-9, 2016.

Article in En | MEDLINE | ID: mdl-27192896

Subject(s)

Factor V/genetics; Infant, Newborn, Diseases/genetics; Methylenetetrahydrofolate Reductase (NADPH2)/genetics; Thrombosis/genetics; Axillary Artery/diagnostic imaging; Female; Humans; Infant, Newborn; Infant, Newborn, Diseases/diagnostic imaging; Mutation; Thrombosis/diagnostic imaging; Ultrasonography

Search on Google

Add to My VHL

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Thrombosis / Factor V / Methylenetetrahydrofolate Reductase (NADPH2) / Infant, Newborn, Diseases Type of study: Diagnostic_studies Limits: Female / Humans / Newborn Language: En Journal: Genet Couns Journal subject: ETICA / GENETICA MEDICA Year: 2016 Document type: Article

Search on Google

Add to My VHL

XML

PubMed Links