217 related articles for article (PubMed ID: 15637993)
1. [Molecular characteristics of the thalassemia syndrome and prenatal diagnosis in a high risk family].
Vujić D; Cvorkov--Drazić M; Pavlović S; Bunjevacki G; Popović Z; Puzigaća Z
Srp Arh Celok Lek; 2001; 129 Suppl 1():56-8. PubMed ID: 15637993
[TBL] [Abstract][Full Text] [Related]
2. [A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].
Zhu BS; He J; Zhang J; Zeng XH; Su J; Xu XH; Li SY; Chen H; Zhang YH
Zhonghua Fu Chan Ke Za Zhi; 2012 Feb; 47(2):85-9. PubMed ID: 22455737
[TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis of beta-thalassaemia mutations using the reverse dot blot technique.
Muralitharan S; Srivastava A; Shaji RV; Mathai M; Srivastava VM; Dennison D; Lu CY; Krishnamoorthy R
Natl Med J India; 1996; 9(2):70-1. PubMed ID: 8857041
[TBL] [Abstract][Full Text] [Related]
4. Analysis of cosegregation of intragenic DNA sequence variations as markers of maternal cell contamination in prenatal diagnosis of β-thalassemia.
Saadi AV; Girisha KM; Gopinath PM; Satyamoorthy K
Transl Res; 2011 Mar; 157(3):150-5. PubMed ID: 21316031
[TBL] [Abstract][Full Text] [Related]
5. Beta-thalassemia in association with a new delta-chain hemoglobin variant [delta116(g18)Arg-->Leu]: implications for carrier screening and prenatal diagnosis.
Waye JS; Patterson M; Walker L; Eng B; Nakamura LM; Lafferty JD; Yong SL; Wu JK; Chui DH
Am J Hematol; 2003 Nov; 74(3):179-81. PubMed ID: 14587045
[TBL] [Abstract][Full Text] [Related]
6. A novel beta-delta globin gene fusion, anti-Lepore Hong Kong, leads to overexpression of delta globin chain and a mild thalassaemia intermedia phenotype when co-inherited with beta(0)-thalassaemia.
So CC; Chan AY; Tsang ST; Lee AC; Au WY; Ma ES; Chan LC
Br J Haematol; 2007 Jan; 136(1):158-62. PubMed ID: 17222202
[TBL] [Abstract][Full Text] [Related]
7. [Diagnostic strategy of beta-thalassemic mutation in a Tunisian family, application in prenatal diagnosis].
Khelil AH; Laradi S; Ferchichi S; Carion N; Béjaoui M; Saad A; Chaieb A; Miled A; Ben Chibani J; Perrin P
Ann Biol Clin (Paris); 2003; 61(2):229-33. PubMed ID: 12702481
[TBL] [Abstract][Full Text] [Related]
8. [A rare thalassemia intermedia case caused by co-existence of Hb H disease (--(SEA)/-alpha(4.2)) and beta-thalassemia major (beta (CD17A)>T/beta (IVS2-654C)>T): implications for prenatal diagnosis].
Li Q; Li LY; Mo QH
Nan Fang Yi Ke Da Xue Xue Bao; 2008 Jan; 28(1):16-9. PubMed ID: 18227017
[TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis of beta-thalassemia in Egypt: implementing accurate high-tech methods did not reflect much on the outcome.
Elgawhary S; Elbaradie Sahar MY; Rashad WM; Mosaad M; Abdalla MA; Ezzat G; Wali YA; Elbeshlawy A
Pediatr Hematol Oncol; 2008 Sep; 25(6):541-8. PubMed ID: 18728973
[TBL] [Abstract][Full Text] [Related]
10. A simple non radioactive method for detecting beta-thalassemia/hbe disease: application to prenatal diagnosis.
Fucharoen S; Fucharoen G; Ratanasiri T; Jetsrisuparb A; Fukumaki Y
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():278-81. PubMed ID: 8629124
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of beta-thalassemia in the West Bank and Gaza.
Ayesh SK; Al-Sharef WA; Nassar SM; Thawabteh NA; Abu-Libdeh BY
Saudi Med J; 2005 Nov; 26(11):1771-6. PubMed ID: 16311664
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of beta-thalassaemia by reverse dot-blot hybridization.
Winichagoon P; Saechan V; Sripanich R; Nopparatana C; Kanokpongsakdi S; Maggio A; Fucharoen S
Prenat Diagn; 1999 May; 19(5):428-35. PubMed ID: 10360511
[TBL] [Abstract][Full Text] [Related]
13. [Genetic diagnosis of alpha and beta thalassemia dual heterozygote].
Zeng R; Yu S; Hu B
Zhonghua Xue Ye Xue Za Zhi; 1998 Oct; 19(10):525-7. PubMed ID: 11189497
[TBL] [Abstract][Full Text] [Related]
14. Establishment of prenatal diagnosis for beta-thalassaemia: a step towards its control in a developing country.
Garewal G; Das R; Jaur J; Marwaha RK; Gupta I
Ann Hum Biol; 2005; 32(2):138-44. PubMed ID: 16096209
[TBL] [Abstract][Full Text] [Related]
15. Variable haematological and clinical presentation of β-thalassaemia carriers and homozygotes with the Poly A (T→C) mutation in the Indian population.
Italia K; Sawant P; Surve R; Wadia M; Nadkarni A; Ghosh K; Colah R
Eur J Haematol; 2012 Aug; 89(2):160-4. PubMed ID: 22690826
[TBL] [Abstract][Full Text] [Related]
16. Profile of beta-thalassemia in eastern India and its prenatal diagnosis.
Bandyopadhyay A; Bandyopadhyay S; Basak J; Mondal BC; Sarkar AA; Majumdar S; Das MK; Chandra S; Mukhopadhyay A; Sanghamita M; Ghosh K; Dasgupta UB
Prenat Diagn; 2004 Dec; 24(12):992-6. PubMed ID: 15614841
[TBL] [Abstract][Full Text] [Related]
17. [A case of prenatal diagnosis of beta-thalassemia by polymerase chain reaction].
Kolesnikova TN; Moliaka IuK; Surin VL; Luk'ianenko AV; Asanov AIu; Tagiev AF; Solov'ev GIa
Genetika; 1992 Dec; 28(12):130-4. PubMed ID: 1363470
[TBL] [Abstract][Full Text] [Related]
18. Mutational spectrum of delta-globin gene in the Portuguese population.
Morgado A; Picanço I; Gomes S; Miranda A; Coucelo M; Seuanes F; Seixas MT; Romão L; Faustino P
Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081
[TBL] [Abstract][Full Text] [Related]
19. Accurate and rapid prenatal diagnosis of the most frequent East Mediterranean beta-thalassemia mutations.
Naja RP; Kaspar H; Shbaklo H; Chakar N; Makhoul NJ; Zalloua PA
Am J Hematol; 2004 Apr; 75(4):220-4. PubMed ID: 15054814
[TBL] [Abstract][Full Text] [Related]
20. A double heterozygote for (deltabeta)0-thalassemia and codons 41/42 (-TTCT) behaves as a homozygote for the frameshift mutation in a Chinese family.
Liao C; Feng Q; Li J; Huang Y; Li D
Hemoglobin; 2007; 31(3):397-400. PubMed ID: 17654080
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]