Factor VIII gene polymorphisms in the Asian Indian population

Haemophilia

Volumn 6, Issue 6, 2000, Pages 625-630

  Chowdhury, M R ^a,b,c,d   Herrmann, F H ^a,b,c,d   Schroder, W ^a,b,c,d   Lambert, C T ^a,b,c,d   Lalloz, M R A ^a,b,c,d   Layton, M ^a,b,c,d   Kumbnani, H K ^a,b,c,d   Kabra, M ^a,b,c,d   Menon, P S N ^a,b,c,d   Verma, I C ^a,b,c,d  

^a ALL INDIA INSTITUTE OF MEDICAL SCIENCES   (India)

^b UNIVERSITY OF GREIFSWALD   (Germany)

^c KING S COLLEGE HOSPITAL   (United Kingdom)

^d UNIVERSITY OF DELHI   (India)

Author keywords

Allelic frequency; Haemophilia A; Heterozygosity; Polymorphism; Short tandem repeats

Indexed keywords

BLOOD CLOTTING FACTOR 8; DINUCLEOTIDE; DNA; TAQ POLYMERASE;

ARTICLE; ASIAN; CHROMOSOME INVERSION; CONTROLLED STUDY; DINUCLEOTIDE REPEAT; DISEASE SEVERITY; DNA FLANKING REGION; DNA POLYMORPHISM; FAMILY; GENE FREQUENCY; GENE MUTATION; GENETIC SCREENING; HEMOPHILIA A; HETEROZYGOSITY; HUMAN; INDIAN; INTRON; MAJOR CLINICAL STUDY; MARKER GENE; POLYMERASE CHAIN REACTION; POPULATION RESEARCH; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SOUTHERN BLOTTING; TANDEM REPEAT;

ALLELES; FACTOR VIII; FEMALE; GENE FREQUENCY; HEMOPHILIA A; HUMANS; INDIA; POLYMORPHISM, GENETIC; TANDEM REPEAT SEQUENCES;

EID: 0033670558     PISSN: 13518216     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2516.2000.00442.x     Document Type: Article

References (20)

1. Inherited bleeding disorders
2. Factor VIII and FIX gene polymorphisms and carrier analysis in indian population
3. A clinically useful probe linked to hemophilia A
4. An improved method of prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences-application to hemophilia A
5. Simple and convenient detection of a HindIII polymorphic site in intron 19 of factor VIII using PCR
6. Haemophilia A diagnosis by analysis of a hypervariable dinucleotide repeat within the factor VIII gene
7. Hemophilia A diagnosis by simultaneous analysis of two variable dinucleotide tandem repeats within the factor VIII gene
8. Utility of XY-amelogenin gene primers for detection of sex chromosomes
9. Report of a joint WHO/WFH meeting on the control of hemophilia: Carrier detection and prenatal diagnosis
10. Recombination between factor VIII. C gene and St14 locus
11. Carrier testing strategy in hemophilia A
12. Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cells
13. Subcycling-PCR for multiplex long-distance amplification of regions with high and low GC content: Amplification to the inversion hotspot in the factor VIII gene
14. Factor VIII gene inversions in severe hemophilia A. Results of an international consortium study
15. Two new markers at DXS115 for genomic diagnosis in hemophilia A
16. Genomic diagnosis of haemophilia A and B in the German democratic Republic
17. The telomeric region of the human X chromosome long arm: Presence of a highly polymorphic DNA marker and analysis of recombination frequency