메뉴 건너뛰기




Volumn 19, Issue 5, 1999, Pages 428-435

Prenatal diagnosis of β-thalassaemia by reverse dot-blot hybridization

Author keywords

Prenatal diagnosis; Reverse dot blot; Thalassaemia

Indexed keywords

ARTICLE; BETA THALASSEMIA; CLINICAL TRIAL; CODON; DIAGNOSTIC ACCURACY; DOT HYBRIDIZATION; FETUS; GENE MUTATION; HETEROZYGOTE; HIGH RISK POPULATION; HOMOZYGOTE; HUMAN; MAJOR CLINICAL STUDY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

EID: 0032961041     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199905)19:5<428::AID-PD563>3.0.CO;2-0     Document Type: Article
Times cited : (70)

References (28)
  • 3
    • 0024596607 scopus 로고
    • Rapid prenatal diagnosis of β-thalassemia using DNA amplification and nonradioactive probes
    • Cai S-P, Chang CA, Zhang J-Z, Saiki RK, Erlich HA, Ran YW. 1989. Rapid prenatal diagnosis of β-thalassemia using DNA amplification and nonradioactive probes. Blood 73: 372-374.
    • (1989) Blood , vol.73 , pp. 372-374
    • Cai, S.-P.1    Chang, C.A.2    Zhang, J.-Z.3    Saiki, R.K.4    Erlich, H.A.5    Ran, Y.W.6
  • 4
    • 0028158097 scopus 로고
    • Reverse dot blot probes for the screening of β-thalassemia mutations in Asians and American Blacks
    • Cai S-P, Wall J, Dan YW, Chehab FF. 1994. Reverse dot blot probes for the screening of β-thalassemia mutations in Asians and American Blacks. Hum Mut 3: 59-63.
    • (1994) Hum Mut , vol.3 , pp. 59-63
    • Cai, S.-P.1    Wall, J.2    Dan, Y.W.3    Chehab, F.F.4
  • 5
    • 0024504090 scopus 로고
    • β thalassaemia mutations in Mediterranean populations
    • Cao A, Gossens M, Pirastu M. 1989. β thalassaemia mutations in Mediterranean populations. Br J Haematol 71: 309-312.
    • (1989) Br J Haematol , vol.71 , pp. 309-312
    • Cao, A.1    Gossens, M.2    Pirastu, M.3
  • 6
    • 0023177954 scopus 로고
    • The molecular basis of β-thalassemia in Lebanon: Application to prenatal diagnosis
    • Chehab FF, Der Kaloustian V, Khouri FP, Deeb SS, Kan YW. 1987. The molecular basis of β-thalassemia in Lebanon: application to prenatal diagnosis. Blood 69: 1141-1145.
    • (1987) Blood , vol.69 , pp. 1141-1145
    • Chehab, F.F.1    Der Kaloustian, V.2    Khouri, F.P.3    Deeb, S.S.4    Kan, Y.W.5
  • 9
    • 0025666527 scopus 로고
    • Methods of detection of single base substitution in clinical genetic practice
    • Forrest S, Cotton RGH. 1990. Methods of detection of single base substitution in clinical genetic practice. Mol Biol Med 7: 451-459.
    • (1990) Mol Biol Med , vol.7 , pp. 451-459
    • Forrest, S.1    Cotton, R.G.H.2
  • 10
    • 0023112573 scopus 로고
    • Hemoglobinopathies in Southeast Asia
    • Fucharoen S, Winichagoon P. 1987. Hemoglobinopathies in Southeast Asia. Hemoglobin 11: 65-88.
    • (1987) Hemoglobin , vol.11 , pp. 65-88
    • Fucharoen, S.1    Winichagoon, P.2
  • 11
    • 0024247865 scopus 로고
    • Problem of thalassemia in Thailand
    • Fucharoen S, Winichagoon P. 1988. Problem of thalassemia in Thailand. ICMR Annals 8: 29-33.
    • (1988) ICMR Annals , vol.8 , pp. 29-33
    • Fucharoen, S.1    Winichagoon, P.2
  • 12
    • 0027078238 scopus 로고
    • Thalassemia in Southeast Asia: Problems and strategy for prevention and control
    • Fucharoen S, Winichagoon P. 1992. Thalassemia in Southeast Asia: problems and strategy for prevention and control. Southeast Asian J Trop Med Public Health 23: 647-655.
    • (1992) Southeast Asian J Trop Med Public Health , vol.23 , pp. 647-655
    • Fucharoen, S.1    Winichagoon, P.2
  • 13
    • 0007752751 scopus 로고    scopus 로고
    • Hemoglobinopathies in Southeast Asia: Molecular biology and clinical medicine
    • Fucharoen S, Winichagoon P. 1997. Hemoglobinopathies in Southeast Asia: molecular biology and clinical medicine. Hemoglobin 21: 299-319.
    • (1997) Hemoglobin , vol.21 , pp. 299-319
    • Fucharoen, S.1    Winichagoon, P.2
  • 17
    • 0027449674 scopus 로고
    • Rapid and simultaneous typing of hemoglobin S, hemoglobin C, and seven Mediterranean β-thalassemia mutations by covalent reverse dot-blot-analysis: Application to prenatal diagnosis in Sicily
    • Maggio A, Giambona A, Cai S-P, Wall J, Kan YW, Chehab FF. 1993. Rapid and simultaneous typing of hemoglobin S, hemoglobin C, and seven Mediterranean β-thalassemia mutations by covalent reverse dot-blot-analysis: application to prenatal diagnosis in Sicily. Blood 81: 239-242.
    • (1993) Blood , vol.81 , pp. 239-242
    • Maggio, A.1    Giambona, A.2    Cai, S.-P.3    Wall, J.4    Kan, Y.W.5    Chehab, F.F.6
  • 19
    • 0028169585 scopus 로고
    • β-thalassemia mutations in Singapore - A strategy for prenatal diagnosis
    • Ng ISL, Ong JBK, Tan CL, Law HY. 1994. β-thalassemia mutations in Singapore - a strategy for prenatal diagnosis. Hum Genet 94: 385-388.
    • (1994) Hum Genet , vol.94 , pp. 385-388
    • Ng, I.S.L.1    Ong, J.B.K.2    Tan, C.L.3    Law, H.Y.4
  • 20
    • 0027611182 scopus 로고
    • Detecting single-base mutations
    • Prosser J. 1993. Detecting single-base mutations. TIB TECH 11: 238-246.
    • (1993) TIB TECH , vol.11 , pp. 238-246
    • Prosser, J.1
  • 21
    • 0023753018 scopus 로고
    • Diagnosis of sickle cell anemia and β-thalassemia with enzymatically amplified DNA and nonradioactive allele-specific oligonucleotide probes
    • Saiki RK, Chang C-A, Levenson CH, Warren TC, Boehm CD, Kazazian HH Jr, Erlich HA. 1988. Diagnosis of sickle cell anemia and β-thalassemia with enzymatically amplified DNA and nonradioactive allele-specific oligonucleotide probes. N Engl J Med 319: 537-541.
    • (1988) N Engl J Med , vol.319 , pp. 537-541
    • Saiki, R.K.1    Chang, C.-A.2    Levenson, C.H.3    Warren, T.C.4    Boehm, C.D.5    Kazazian H.H., Jr.6    Erlich, H.A.7
  • 22
    • 0001442557 scopus 로고
    • Genetic analysis of amplified DNA with immobilized sequence-specific oligonucleotide probes
    • Saiki RK, Walsh PS, Levenson CH, Erlich HA. 1989. Genetic analysis of amplified DNA with immobilized sequence-specific oligonucleotide probes. Proc Natl Acad Sci USA 86: 6230-6234.
    • (1989) Proc Natl Acad Sci USA , vol.86 , pp. 6230-6234
    • Saiki, R.K.1    Walsh, P.S.2    Levenson, C.H.3    Erlich, H.A.4
  • 24
    • 0025887115 scopus 로고
    • The spectrum of β-thalassaemia mutations on the Indian subcontinent: The basis for prenatal diagnosis
    • Varawalla NY, Old JM, Sarkar R, Venkatesan R, Weatherall DJ. 1991. The spectrum of β-thalassaemia mutations on the Indian subcontinent: the basis for prenatal diagnosis. Br J Haematol 78: 242-247.
    • (1991) Br J Haematol , vol.78 , pp. 242-247
    • Varawalla, N.Y.1    Old, J.M.2    Sarkar, R.3    Venkatesan, R.4    Weatherall, D.J.5
  • 25
    • 0030754149 scopus 로고    scopus 로고
    • Regional distribution of β-thalassemia mutations in India
    • Verma IC, Saxena R, Thomas E, Jain PK. 1997. Regional distribution of β-thalassemia mutations in India. Hum Genet 100: 109-113.
    • (1997) Hum Genet , vol.100 , pp. 109-113
    • Verma, I.C.1    Saxena, R.2    Thomas, E.3    Jain, P.K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.