Prenatal diagnosis of haemophilia: Our experience of 44 cases

Clinical Chemistry and Laboratory Medicine

Volumn 51, Issue 12, 2013, Pages 2233-2238

  Zarrilli, Federica ^a,b   Sanna, Veronica ^a,b   Ingino, Rosaria ^a,b   Santamaria, Rita ^b   Rocino, Angiola ^c   Coppola, Antonio ^b   Di Minno, Giovanni ^b   Castaldo, Giuseppe ^a,b  

^a CEINGE BIOTECNOLOGIE AVANZATE   (Italy)

^b UNIVERSITY OF NAPLES FEDERICO II   (Italy)

^c Centro Emofilia e Trombosi   (Italy)

Author keywords

Amniocentesis; Chorionic villi; F8C; F9; Haemophilia; Prenatal diagnosis

Indexed keywords

DNA;

AMNIOCENTESIS; ARTICLE; CLINICAL ARTICLE; DENATURING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; DNA SEQUENCE; FEMALE; GENE MUTATION; GENE SEQUENCE; HEMOPHILIA A; HEMOPHILIA B; HUMAN; INDUCED ABORTION; INTRON; KARYOTYPE; LINKAGE ANALYSIS; MALE; MOLECULAR DIAGNOSIS; MOSAICISM; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; Y CHROMOSOME;

FEMALE; GENETIC COUNSELING; HEMOPHILIA A; HUMANS; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 84884598545     PISSN: 14346621     EISSN: 14374331     Source Type: Journal    
DOI: 10.1515/cclm-2013-0205     Document Type: Article

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