Carrier detection and prenatal diagnosis of hemophilia A

Clinical Chemistry and Laboratory Medicine

Volumn 39, Issue 12, 2001, Pages 1204-1208

  Xuefeng, W ^a   Yuanfang, L ^a   Zhiguang, L ^a   Haiyan, C ^a   Xiaojie, S ^a   Yishi, F ^a   Hongli, W ^a  

^a SHANGHAI SECOND MEDICAL UNIVERSITY   (China)

Author keywords

Hemophilia A; Prenatal diagnosis

Indexed keywords

BLOOD CLOTTING FACTOR 8; ONCOPROTEIN;

ARTICLE; CHROMOSOME INVERSION; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; FETUS; GENE LOCUS; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC POLYMORPHISM; HEMOPHILIA A; HEREDITY; HETEROZYGOTE DETECTION; HUMAN; INTRON; MALE; MEDICAL ASSESSMENT; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; TANDEM REPEAT; VARIABLE NUMBER OF TANDEM REPEAT;

BASE SEQUENCE; CHROMOSOME MAPPING; FEMALE; GENETIC MARKERS; HEMOPHILIA A; HETEROZYGOTE; HETEROZYGOTE DETECTION; HUMANS; INTRONS; INVERSION, CHROMOSOME; MALE; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; PREGNANCY; PRENATAL DIAGNOSIS; SEQUENCE DELETION; TANDEM REPEAT SEQUENCES;

EID: 0035664022     PISSN: 14346621     EISSN: None     Source Type: Journal    
DOI: 10.1515/CCLM.2001.191     Document Type: Article

References (8)

1. Hereditary hemal diseases
2. Single-tube polymerase chain reaction for rapid diagnosis of inversion mutation in hemophilia A
3. The study on frequency distribution of DXS52 VNTR locus polymorphism
4. The application of DXS52(DXS52) VNTR locus in hemaphilia A gene diagnosis in normal people of North-West China
5. Genetic mapping and diagnosis of hemophilia A achieved through a Bcl I polymorphism in the factor VIII gene
6. Analysis of Bcl I polymorphism of factor VIII gene in the molecular diagnosis of hemophilia A carriers in families from northwestern Venezuela
7. Haemophilia A diagnosis by mutations analysis of two variable dinucleotide tandem repeats within the Factor VIII gene