189 related articles for article (PubMed ID: 9332092)
1. Hemoglobin E-beta thalassemia in Uttar Pradesh.
Agarwal S; Gulati R; Singh K
Indian Pediatr; 1997 Apr; 34(4):287-92. PubMed ID: 9332092
[TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis of beta-thalassemia/Hb E by hemoglobin typing compared to DNA analysis.
Sirichotiyakul S; Saetung R; Sanguansermsri T
Hemoglobin; 2009; 33(1):17-23. PubMed ID: 19205969
[TBL] [Abstract][Full Text] [Related]
3. Prevention of homozygous beta thalassemia by premarital screening and prenatal diagnosis in India.
Tamhankar PM; Agarwal S; Arya V; Kumar R; Gupta UR; Agarwal SS
Prenat Diagn; 2009 Jan; 29(1):83-8. PubMed ID: 19090545
[TBL] [Abstract][Full Text] [Related]
4. Hemoglobin E-beta thalassemia: factors affecting phenotype.
Panigrahi I; Agarwal S; Gupta T; Singhal P; Pradhan M
Indian Pediatr; 2005 Apr; 42(4):357-62. PubMed ID: 15876597
[TBL] [Abstract][Full Text] [Related]
5. Application of maternal plasma DNA analysis for noninvasive prenatal diagnosis of Hb E-beta-thalassemia.
Tungwiwat W; Fucharoen G; Fucharoen S; Ratanasiri T; Sanchaisuriya K; Sae-Ung N
Transl Res; 2007 Nov; 150(5):319-25. PubMed ID: 17964521
[TBL] [Abstract][Full Text] [Related]
6. [Phenotype and genotype analysis of hemoglobin E].
Li YQ; Huang HP; Qin GF; Yang WH; Lao ZC
Zhonghua Xue Ye Xue Za Zhi; 2012 Oct; 33(10):861-4. PubMed ID: 23384913
[TBL] [Abstract][Full Text] [Related]
7. The clinical significance of the spectrum of interactions of CAP+1 (A-->C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians.
Garewal G; Das R; Awasthi A; Ahluwalia J; Marwaha RK
Eur J Haematol; 2007 Nov; 79(5):417-21. PubMed ID: 17900295
[TBL] [Abstract][Full Text] [Related]
8. Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases.
Srivorakun H; Fucharoen G; Sae-Ung N; Sanchaisuriya K; Ratanasiri T; Fucharoen S
Eur J Haematol; 2009 Jul; 83(1):57-65. PubMed ID: 19226360
[TBL] [Abstract][Full Text] [Related]
9. Molecular and hematological characterization of HPFH-6/Indian deletion-inversion Ggamma(Agammadeltabeta)0-thalassemia and Ggamma(Agammadeltabeta)0-thalassemia/HbE in Thai patients.
Fucharoen S; Pengjam Y; Surapot S; Fucharoen G; Sanchaisuriya K
Am J Hematol; 2002 Oct; 71(2):109-13. PubMed ID: 12353310
[TBL] [Abstract][Full Text] [Related]
10. Inherited hemoglobin disorders in Andhra Pradesh, India: a population study.
Munshi A; Anandraj MP; Joseph J; Shafi G; Anila AN; Jyothy A
Clin Chim Acta; 2009 Feb; 400(1-2):117-9. PubMed ID: 19000664
[TBL] [Abstract][Full Text] [Related]
11. Variable clinical severity of Hb E beta-thalassemia among Indians.
Nadkarni A; Ghosh K; Gorakshakar A; Colah R; Mohanty D
J Assoc Physicians India; 1999 Oct; 47(10):966-8. PubMed ID: 10778688
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis for beta-thalassemia syndromes using HRP-labeled oligonucleotide probes at Siriraj Hospital.
Winichagoon P; Fucharoen S; Siritanaratkul N; Tassana P; Thonglairoam V; Siriboon W; Kanokpongsakdi S
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():282-6. PubMed ID: 8629125
[TBL] [Abstract][Full Text] [Related]
13. The spectrum of beta-thalassemia mutations in Malays in Singapore and Kelantan.
Abdullah WA; Jamaluddin NB; Kham SK; Tan JA
Southeast Asian J Trop Med Public Health; 1996 Mar; 27(1):164-8. PubMed ID: 9031421
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Screening of Iranian thalassemic families for the most common deletions of the beta-globin gene cluster.
Esteghamat F; Imanian H; Azarkeivan A; Pourfarzad F; Almadani N; Najmabadi H
Hemoglobin; 2007; 31(4):463-9. PubMed ID: 17994380
[TBL] [Abstract][Full Text] [Related]
16. Clinical and hematological phenotype of homozygous hemoglobin E: revisit of a benign condition with hidden reproductive risk.
Tachavanich K; Viprakasit V; Chinchang W; Glomglao W; Pung-Amritt P; Tanphaichitr VS
Southeast Asian J Trop Med Public Health; 2009 Mar; 40(2):306-16. PubMed ID: 19323016
[TBL] [Abstract][Full Text] [Related]
17. Interaction of hemoglobin E and several forms of alpha-thalassemia in Cambodian families.
Fucharoen S; Sanchaisuriya K; Fucharoen G; Panyasai S; Devenish R; Luy L
Haematologica; 2003 Oct; 88(10):1092-8. PubMed ID: 14555303
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [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]
20. Spectrum of hemoglobinopathies in the state of Orissa, India: a ten years cohort study.
Balgir RS
J Assoc Physicians India; 2005 Dec; 53():1021-6. PubMed ID: 16572956
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]