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168 related items for PubMed ID: 7927334
21. Rapid screening of multiple beta-globin gene mutations by real-time PCR on the LightCycler: application to carrier screening and prenatal diagnosis of thalassemia syndromes. Vrettou C, Traeger-Synodinos J, Tzetis M, Malamis G, Kanavakis E. Clin Chem; 2003 May; 49(5):769-76. PubMed ID: 12709368 [Abstract] [Full Text] [Related]
22. [Beta-thalassemia major caused by compound heterozygosity for +40 to +43(-AAAC), IVS-2-654 (C to T) and codon 41/42 (-TCTT)]. Hu ZH, Liu YL, Zeng ZY, Zhang XL, Zhu QY. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Aug; 25(4):418-20. PubMed ID: 18683140 [Abstract] [Full Text] [Related]
23. [Molecular-genetic characteristics of alpha, beta and delta beta-thalassemias in 139 heterozygotes in 56 unrelated Czech and Slovak families (Priority description of 3 beta-thalassemia mutations, an extensive alpha-thalassemia 2 (18+ kb) deletion and a Swiss-type nondeletion hereditary persistence of hemoglobin F)]. Indrák K, Divoký V, Brabec V, Indráková J, Svobodová M, Huisman TH. Vnitr Lek; 1993 Oct; 39(10):969-78. PubMed ID: 7694425 [Abstract] [Full Text] [Related]
24. Identification of three novel mutations [-41 (A>C), codon 24 (-G), and IVS-I-109 (-T)], in a study of beta-thalassemia alleles in the Isfahan region of Iran. Salehi R, Fisher CA, Bignell PA, Eslami G, Old JM. Hemoglobin; 2010 Oct; 34(1):115-20. PubMed ID: 20113296 [Abstract] [Full Text] [Related]
25. [Analysis of beta-thalassemia mutations and prenated diagnosis in Chengdu population]. Liu B, Fang J, Liu S, Ouyang X, Wang F, Liu L, Ma C, Huo P, Li Y. Hua Xi Yi Ke Da Xue Xue Bao; 1995 Dec; 26(4):361-6. PubMed ID: 8732052 [Abstract] [Full Text] [Related]
26. Study of beta-Thalassemia mutations using the polymerase chain reaction-amplification refractory mutation system and direct DNA sequencing techniques in a group of Egyptian Thalassemia patients. El-Gawhary S, El-Shafie S, Niazi M, Aziz M, El-Beshlawy A. Hemoglobin; 2007 Dec; 31(1):63-9. PubMed ID: 17365006 [Abstract] [Full Text] [Related]
27. Rapid and simultaneous typing of hemoglobin S, hemoglobin C, and seven Mediterranean beta-thalassemia mutations by covalent reverse dot-blot analysis: application to prenatal diagnosis in Sicily. Maggio A, Giambona A, Cai SP, Wall J, Kan YW, Chehab FF. Blood; 1993 Jan 01; 81(1):239-42. PubMed ID: 8417793 [Abstract] [Full Text] [Related]
28. Sistani population: a different spectrum of β-thalassemia mutations from other ethnic groups of Iran. Miri-Moghaddam E, Zadeh-Vakili A, Nikravesh A, Sistani SS, Naroie-Nejad M. Hemoglobin; 2013 Jan 01; 37(2):138-47. PubMed ID: 23437895 [Abstract] [Full Text] [Related]
29. Detection of beta-globin gene mutations by polymerase chain reaction. Lee HH, Chang JG, Lee LS, Lin ST, Ko TM, Choo KB. Proc Natl Sci Counc Repub China B; 1991 Apr 01; 15(2):97-100. PubMed ID: 1682965 [Abstract] [Full Text] [Related]
30. Molecular characterization of alpha-thalassemia determinants, beta-thalassemia alleles, and beta S haplotypes among Kuwaiti Arabs. Adekile AD, Gu LH, Baysal E, Haider MZ, al-Fuzae L, Aboobacker KC, al-Rashied A, Huisman TH. Acta Haematol; 1994 Apr 01; 92(4):176-81. PubMed ID: 7701914 [Abstract] [Full Text] [Related]
32. Molecular basis of beta-thalassemia in Japan: heterogeneity and origins of mutations. Wakamatsu C, Ichinose M, Manabe J, Fucharoen S, Sawada H, Ohga S, Nishimura J, Nukina H, Harada T, Shirahata S. Acta Haematol; 1994 Apr 01; 91(3):136-43. PubMed ID: 8091935 [Abstract] [Full Text] [Related]
33. 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 01; 75(4):220-4. PubMed ID: 15054814 [Abstract] [Full Text] [Related]
34. [Molecular and prenatal diagnosis for a Chinese pregnant woman with a novel mutation of β thalassemia]. Hao Y, Xu ZY, Jin Q, Wu WQ, Cai J, Luo CQ, Xie JS. Zhonghua Xue Ye Xue Za Zhi; 2011 Apr 01; 32(4):245-8. PubMed ID: 21569707 [Abstract] [Full Text] [Related]