Carrier detection and prenatal diagnosis of hemophilia in developing countries

Seminars in Thrombosis and Hemostasis

Volumn 31, Issue 5, 2005, Pages 544-554

  Peyvandi, Flora ^a  

^a FONDAZIONE IRCCS CA GRANDA OSPEDALE MAGGIORE POLICLINICO   (Italy)

Author keywords

Carrier detection; Factor IX; Factor VIII; Genetic analysis; Hemophilia A and B; Prenatal diagnosis

Indexed keywords

BLOOD CLOTTING FACTOR 8; BLOOD CLOTTING FACTOR 9; DNA;

AFRICAN AMERICAN; ASIAN; BLEEDING DISORDER; BRAZIL; CAUCASIAN; CHINESE; CONTROLLED STUDY; DEVELOPING COUNTRY; ETHNIC GROUP; F8 GENE; F9 GENE; GENE; GENE MUTATION; GENETIC ANALYSIS; GENETIC DISORDER; GENETIC LINKAGE; GENETIC MARKER; GENETIC SCREENING; GEOGRAPHIC DISTRIBUTION; HEMOPHILIA; HEMOPHILIA A; HEMOPHILIA B; HETEROZYGOTE DETECTION; HUMAN; HUMAN CELL; INDIAN; JAPANESE; MOLECULAR BIOLOGY; PRENATAL DIAGNOSIS; PREVALENCE; PRIORITY JOURNAL; REVIEW; RUSSIAN FEDERATION; X CHROMOSOME RECESSIVE INHERITANCE;

DEVELOPING COUNTRIES; FEMALE; GENETIC SCREENING; HEMOPHILIA A; HETEROZYGOTE DETECTION; HUMANS; MALE; MUTATION; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 27844606354     PISSN: 00946176     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-922226     Document Type: Review

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