The use of DNA markers for carrier detection and prenatal diagnosis of haemophilia A in Egyptian families

Haemophilia

Volumn 14, Issue 5, 2008, Pages 1082-1087

  Hussein, Ibtessam Ramzi ^a   El beshlawy, A ^b   Salem, A ^c   Mosaad, R ^a   Zaghloul, N ^b   Ragab, L ^b   Fayek, H ^a   Gaber, K ^a   El ekiabi, M ^d  

^a NATIONAL RESEARCH CENTRE   (Egypt)

^b CAIRO UNIVERSITY   (Egypt)

^c Ain Shams University   (Egypt)

^d Shabrawishi Hospital   (Egypt)

Author keywords

Carrier detection; DNA markers; Factor VIII; Haemophilia A

Indexed keywords

DNA;

ARTICLE; CONTROLLED STUDY; DIAGNOSTIC ACCURACY; DIAGNOSTIC VALUE; EGYPT; FAMILY; FEMALE; FETUS; GENE LOCUS; GENETIC MARKER; GENETIC SCREENING; HEMOPHILIA A; HETEROZYGOSITY; HETEROZYGOTE DETECTION; HUMAN; INTRON; LINKAGE ANALYSIS; MAJOR CLINICAL STUDY; MALE; MOTHER; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; RESTRICTION MAPPING; RESTRICTION SITE; VARIABLE NUMBER OF TANDEM REPEAT;

FACTOR VIII; FEMALE; FETAL DISEASES; GENETIC MARKERS; HEMOPHILIA A; HETEROZYGOTE DETECTION; HUMANS; LINKAGE (GENETICS); MALE; MINISATELLITE REPEATS; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 51249116228     PISSN: 13518216     EISSN: 13652516     Source Type: Journal    
DOI: 10.1111/j.1365-2516.2008.01779.x     Document Type: Article

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