Carrier detection by DNA linkage analysis in eighty Thai hemophilia A families

Journal of the Medical Association of Thailand

Volumn 85, Issue SUPPL. 2, 2002, Pages

  Mahasandana, Chularatana ^a   Treesucon, Ajjima ^a   Veerakul, Gavivann ^a   Yenchitsomanus, Pa Thai ^a   Pung Amritt, Parichat ^a   Petrarat, Siripan ^a   Visudhiphan, Sukon ^a  

^a MAHIDOL UNIVERSITY   (Thailand)

Author keywords

Carrier Detection; DNA Linkage Analysis; Factor VIII Gene; Hemophilia A

Indexed keywords

ADULT; ARTICLE; CHILD; COHORT ANALYSIS; FEMALE; GENETIC LINKAGE; GENETIC POLYMORPHISM; GENETICS; HEMOPHILIA A; HETEROZYGOTE; HETEROZYGOTE DETECTION; HUMAN; MALE; METHODOLOGY; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PEDIGREE; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; RETROSPECTIVE STUDY; THAILAND;

ADULT; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; COHORT STUDIES; DNA MUTATIONAL ANALYSIS; FEMALE; HEMOPHILIA A; HETEROZYGOTE; HETEROZYGOTE DETECTION; HUMANS; LINKAGE (GENETICS); MALE; MOLECULAR SEQUENCE DATA; PEDIGREE; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; RETROSPECTIVE STUDIES; THAILAND;

EID: 0036690471     PISSN: 01252208     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (21)

1. Isarangkura P, Hathirat P, Watana-Kasetr S, et al. Study of the prevalence of hereditary bleeding disorders in Thailand. Vajira Med Journal 1980; 24: 183-9.
2. Gitschier J, Wood WI, Goralka TM, et al. Characterization of the human factor VIII gene. Nature 1984; 312: 326-30.
3. Wood WI, Capon DJ, Simosen CC, et al. Expression of active human factor VIII from recombinant DNA clones. Nature 1984; 312: 330-7.
4. Toole JJ, Knopf JL, Wozney JM, et al. Molecular cloning of cDNA encoding human antihaemophilic factor. Nature 1984; 312: 342-7.
5. Thompson AR. Molecular biology of the hemophilias. Prog Hemost Thromb 1991; 10: 175-214.
6. Peake IR, Lillicrap DP, Boulyjenkov V, et al. Haemophilia: Strategies for carrier detection and prenatal diagnosis. Bull World Health Organ 1993; 71: 429-58.
7. Tuddenham EGD, Schwaab R, Seekafer J, et al. Hemophilia A: Data base of nucleotide substitutions, deletions, insertions and rearrangement of the factor VIII gene. Nucleic Acids Res 1994; 22: 3511-33.
8. Goodeve AC, Chuansumrit A, Sasanakul W, et al. A comparison of the allelic frequencies of ten DNA polymorphisms associated with factor VIII and Factor IX genes in Thai and Western European populations. Blood Coag Fribrinol 1994; 5: 29-35.
9. Yang YH, Song KS, Kim IK, Cha DH. Rapid polymerase chain-reaction analysis of St 14 (DXS 52) VNTR: Carrier detection of hemophilia A. J Obstet Gynaecol Res 1997; 23: 4: 3399-406.
10. Lalloz MRA, Mc Vey JH, Pattinson JK, Tuddenham EGD. Haemophilia A diagnosis by analysis of a hypervariable dinucleotide repeat within the factor VIII gene. Lancet 1991; 338: 207-11.
11. Hughes AE. Optimization of microsatellite analysis for genetic mapping. Genomics 1993; 15: 433-4.
12. Lalloz MRA, Schwaab R, Mc Vey JH, Michaelides K, Tuddenham EGD. Hemophilia A diagnosis by simultaneous analysis of two variable dinucleotide tandem repeats within the factor VIII gene. Brit J Haematol 1994; 86: 804-9.
13. Gitschier J, Drayna D, Tuddenham EGD, White RL, Lawn RM. Genetic mapping and diagnosis of haemophila A achieved through a Bd I polymorphism in the factor VIII gene. Nature 1985; 314: 738-40.
14. Kogan SC, Gitschier J. Genetic prediction of hemophilia A. PCR protocol: A guide of methods and application. San Diago: Academic Press 1990; 35: 288-99.
15. Richards B, Heilig R, Oberle I, Storjohann L, Horn GT. Rapid PCR analysis of the ST14 (DXS 52) VNTR. Nucleic Acid Res 1991; 19: 1944.
16. Wion KL, Tuddenham EGD, Lawn RM. A new polymorphism in the factor VIII gene for prenatal diagnosis of hemophilia A. Nuclic Acids Res 1986; 14: 4535-42.
17. Ahrens P, Kruse TA, Schwartz M, Rasmussen PB, Din N. A new Hind III restriction fragment length polymorphism in the hemophilia A locus. Hum Genet 1987; 76: 127-8.
18. Oberle I, Camerino G, Heilig R, et al. Genetic screening of hemophilia A (classic hemophilia) with a polymorphic DNA probe. N Engl J Med 1985; 312: 682-6.
19. Windsor S, Taylor SAM, Lillicrap D. Multiplex analysis of two intragenic microsatellite repeat polymorphisms in the genetic diagnosis of hemophilia A. Br J Haematol 1994; 86: 810-5.
20. Dangerfield BTF, Manga P, Field SP, et al. Feasibility of prenatal diagnosis and carrier detection in South African hemophilia A patients. Br J Haematol 1997; 97: 558-60.
21. Yip B, Chan V, Chan TK. Intragenic dinucleotide repeats in factor VIII gene for the diagnosis of hemophilia A. Br J Haematol 1994; 88: 889-91.