-
1
-
-
33845712099
-
-
1 st ed. Shiraz University of Medical Sciences Publishing Center: Shiraz;, Book in Persian
-
Haghshenas M, Zamani J. Thalassemia. 1 st ed. Shiraz University of Medical Sciences Publishing Center: Shiraz; 1997. [Book in Persian].
-
(1997)
Thalassemia
-
-
Haghshenas, M.1
Zamani, J.2
-
2
-
-
33645711639
-
Fourteen-year experience of prenatal diagnosis of thalassemia in Iran
-
Najmabadi H, Ghamari A, Sahebjam F, Kariminejad R, Hadavi V, Khatibi T, et al. Fourteen-year experience of prenatal diagnosis of thalassemia in Iran. Comm Gen 2006;9:93-7.
-
(2006)
Comm Gen
, vol.9
, pp. 93-97
-
-
Najmabadi, H.1
Ghamari, A.2
Sahebjam, F.3
Kariminejad, R.4
Hadavi, V.5
Khatibi, T.6
-
3
-
-
0032861759
-
Prevalence study and molecular characterization of alpha thalassemia in Filipinos
-
Ko TM, Hwa HL, Liu CW, Li SF, Chu JY, Cheung YP. Prevalence study and molecular characterization of alpha thalassemia in Filipinos. Ann Hematol 1999;78:355-7.
-
(1999)
Ann Hematol
, vol.78
, pp. 355-357
-
-
Ko, T.M.1
Hwa, H.L.2
Liu, C.W.3
Li, S.F.4
Chu, J.Y.5
Cheung, Y.P.6
-
4
-
-
14644437152
-
Prevalence of alpha-globin gene deletions among patients with unexplained microcytosis in a north-American population
-
Bergeron J, Weng X, Robin L, Olney HJ, Soulieres D. Prevalence of alpha-globin gene deletions among patients with unexplained microcytosis in a north-American population. Hemoglobin 2005;29:51-60.
-
(2005)
Hemoglobin
, vol.29
, pp. 51-60
-
-
Bergeron, J.1
Weng, X.2
Robin, L.3
Olney, H.J.4
Soulieres, D.5
-
6
-
-
0036819603
-
Rapid detection of a+ thalassemia deletion and ß- globin gene triplication by GAP-PCR in Indian subjects
-
Agarwal S, Sarwai S, Nigam N, Singhal P. Rapid detection of a+ thalassemia deletion and ß- globin gene triplication by GAP-PCR in Indian subjects. Indian J Med Res 2002;116:155-61.
-
(2002)
Indian J Med Res
, vol.116
, pp. 155-161
-
-
Agarwal, S.1
Sarwai, S.2
Nigam, N.3
Singhal, P.4
-
7
-
-
0024605518
-
Analysis of any point mutation in DNA: The amplification refractory mutation system (ARMS)
-
Newton CR, Graham A, Heptinstall LE, Powell SJ, Summers C, Kalsheker N, et al. Analysis of any point mutation in DNA: The amplification refractory mutation system (ARMS). Nucleic Acids Res 1989;17:2503-16.
-
(1989)
Nucleic Acids Res
, vol.17
, pp. 2503-2516
-
-
Newton, C.R.1
Graham, A.2
Heptinstall, L.E.3
Powell, S.J.4
Summers, C.5
Kalsheker, N.6
-
8
-
-
0025090944
-
Rapid detection and prenatal diagnosis of ß-thalassemia: Studies in Indian and Cypriot populations in the UK
-
Old JM, Varawalla NY, Weatherall DJ. Rapid detection and prenatal diagnosis of ß-thalassemia: Studies in Indian and Cypriot populations in the UK. Lancet 1990;336:834-7.
-
(1990)
Lancet
, vol.336
, pp. 834-837
-
-
Old, J.M.1
Varawalla, N.Y.2
Weatherall, D.J.3
-
9
-
-
0027939006
-
The amplification refractory mutation system (ARMS): A rapid and direct prenatal diagnostic technique for beta-thalassemia in Singapore
-
Tan JA, Tay JS, Lin LI, Kham SK, Chia JN, Chin TM, et al. The amplification refractory mutation system (ARMS): A rapid and direct prenatal diagnostic technique for beta-thalassemia in Singapore. Prenat Diagn 1994;14:1077-82.
-
(1994)
Prenat Diagn
, vol.14
, pp. 1077-1082
-
-
Tan, J.A.1
Tay, J.S.2
Lin, L.I.3
Kham, S.K.4
Chia, J.N.5
Chin, T.M.6
-
10
-
-
0033983971
-
Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemia
-
Chong SS, Boehm CD, Higgs DR, Cutting GR. Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemia. Blood 2000;95:360-2.
-
(2000)
Blood
, vol.95
, pp. 360-362
-
-
Chong, S.S.1
Boehm, C.D.2
Higgs, D.R.3
Cutting, G.R.4
-
11
-
-
0034091983
-
Rapid detection of alpha-thalassemia deletions and alpha-globin gene triplication by multiplex polymerase chain reactions
-
Liu YT, Old JM, Miles K, Fisher CA, Weatherall DJ, Clegg JB. Rapid detection of alpha-thalassemia deletions and alpha-globin gene triplication by multiplex polymerase chain reactions. Br J Haematol 2000;108:295-9.
-
(2000)
Br J Haematol
, vol.108
, pp. 295-299
-
-
Liu, Y.T.1
Old, J.M.2
Miles, K.3
Fisher, C.A.4
Weatherall, D.J.5
Clegg, J.B.6
-
12
-
-
0034091983
-
Rapid detection of a-thalassemia deletions and -globin gene triplication by multiplex polymerase Chain reactions
-
Liu YT, Old JM, Miles K, Fisher CA, Weatherall DJ, Clegg JB. Rapid detection of a-thalassemia deletions and -globin gene triplication by multiplex polymerase Chain reactions. Br J Haematol 2000;108:295-9.
-
(2000)
Br J Haematol
, vol.108
, pp. 295-299
-
-
Liu, Y.T.1
Old, J.M.2
Miles, K.3
Fisher, C.A.4
Weatherall, D.J.5
Clegg, J.B.6
-
14
-
-
0028263783
-
Detection of common deletional a-thalassemia -2 determinants by PCR
-
Baysal E, Huisman TH. Detection of common deletional a-thalassemia -2 determinants by PCR. Am J Hematol 1994;46:208-13.
-
(1994)
Am J Hematol
, vol.46
, pp. 208-213
-
-
Baysal, E.1
Huisman, T.H.2
-
15
-
-
0348110520
-
Determination of the breakpoint and molecular diagnosis of a common -thalassemia -1 deletion in the Indian population
-
Shaji RV, Eunice SE, Baidya S, Srivastava A, Chandy M. Determination of the breakpoint and molecular diagnosis of a common -thalassemia -1 deletion in the Indian population. Br J Haematol 2003;123:942-7.
-
(2003)
Br J Haematol
, vol.123
, pp. 942-947
-
-
Shaji, R.V.1
Eunice, S.E.2
Baidya, S.3
Srivastava, A.4
Chandy, M.5
-
16
-
-
34548782639
-
Elucidating the spectrum of a-thalassemia mutations in Iran
-
Hadavi V, Taromchi AH, Malekpour M, Gholami B, Law HY, Almadani N, et al. Elucidating the spectrum of a-thalassemia mutations in Iran. Haematologica 2007;92:992-3.
-
(2007)
Haematologica
, vol.92
, pp. 992-993
-
-
Hadavi, V.1
Taromchi, A.H.2
Malekpour, M.3
Gholami, B.4
Law, H.Y.5
Almadani, N.6
-
17
-
-
0034852845
-
The beta-thalassemia mutation spectrum in the Iranian population
-
Najmabadi H, Karimi-Nejad R, Sahebjam S, Pourfarzad F, Teimourian S, Sahebjam F, et al. The beta-thalassemia mutation spectrum in the Iranian population. Hemoglobin 2001;25:285-96.
-
(2001)
Hemoglobin
, vol.25
, pp. 285-296
-
-
Najmabadi, H.1
Karimi-Nejad, R.2
Sahebjam, S.3
Pourfarzad, F.4
Teimourian, S.5
Sahebjam, F.6
-
18
-
-
0036797482
-
Rare and unexpected utations among Iranian b-thalassemia patients and prenatal samples discovered by reverse-hybridization and DNA sequencing
-
Najmabadi H, Pourfathollah AA, Neishabury M, Sahebjam F, Krugluger W, Oberkanins C. Rare and unexpected utations among Iranian b-thalassemia patients and prenatal samples discovered by reverse-hybridization and DNA sequencing. Haematologica 2002;87:1113-4.
-
(2002)
Haematologica
, vol.87
, pp. 1113-1114
-
-
Najmabadi, H.1
Pourfathollah, A.A.2
Neishabury, M.3
Sahebjam, F.4
Krugluger, W.5
Oberkanins, C.6
-
19
-
-
14644437152
-
Prevalence of alpha-globin gene deletions among patients with unexplained microcytosis in a north-American population
-
Bergeron J, Weng X, Robin L, Olney HJ, Soulieres D. Prevalence of alpha-globin gene deletions among patients with unexplained microcytosis in a north-American population. Hemoglobin 2005;29:51-60.
-
(2005)
Hemoglobin
, vol.29
, pp. 51-60
-
-
Bergeron, J.1
Weng, X.2
Robin, L.3
Olney, H.J.4
Soulieres, D.5
-
20
-
-
0031453924
-
Feasibility of molecular diagnosis of a- thalassemia in the evaluation of microcytosis
-
Sivera P, Roetto A, Mazza U, Camaschella C. Feasibility of molecular diagnosis of a- thalassemia in the evaluation of microcytosis. Haematologica 1997;82:592-3.
-
(1997)
Haematologica
, vol.82
, pp. 592-593
-
-
Sivera, P.1
Roetto, A.2
Mazza, U.3
Camaschella, C.4
-
22
-
-
0035377422
-
High prevalence of a-thalassemia among individuals with microcytosis and hypochromia without anemia
-
Borges E, Wenning MR, Kimura EM, Gervasio SA, Costa FF, Sonati MF. High prevalence of a-thalassemia among individuals with microcytosis and hypochromia without anemia. Braz J Med Biol Res 2001;34:759-62.
-
(2001)
Braz J Med Biol Res
, vol.34
, pp. 759-762
-
-
Borges, E.1
Wenning, M.R.2
Kimura, E.M.3
Gervasio, S.A.4
Costa, F.F.5
Sonati, M.F.6
-
23
-
-
43449120116
-
Rapid genotyping of known mutations and polymorphisms in ß-globin gene based on the DHPLC profile patterns of homoduplexes and heteroduplexes
-
Li Q, Li LY, Huang SW, Li L, Chen XW, Zhou WJ, et al. Rapid genotyping of known mutations and polymorphisms in ß-globin gene based on the DHPLC profile patterns of homoduplexes and heteroduplexes. Clin Biochem 2008;41:681-7.
-
(2008)
Clin Biochem
, vol.41
, pp. 681-687
-
-
Li, Q.1
Li, L.Y.2
Huang, S.W.3
Li, L.4
Chen, X.W.5
Zhou, W.J.6
-
24
-
-
33947370854
-
High-throughput microtiter well-based chemiluminometric genotyping of 15 HBB gene mutations in a dry-reagent format
-
Glynou K, Kastanis P, Boukouvala S, Tsaoussis V, Ioannou PC, Christopoulos TK, et al. High-throughput microtiter well-based chemiluminometric genotyping of 15 HBB gene mutations in a dry-reagent format. Clin Chem 2007;53:384-91.
-
(2007)
Clin Chem
, vol.53
, pp. 384-391
-
-
Glynou, K.1
Kastanis, P.2
Boukouvala, S.3
Tsaoussis, V.4
Ioannou, P.C.5
Christopoulos, T.K.6
-
25
-
-
50549101788
-
Comparison of the mismatch-specific endonuclease method and denaturing high-performance liquid chromatography for the identification of HBB gene mutations
-
Hung CC, Su YN, Lin CY, Chang YF, Chang CH, Cheng WF, et al. Comparison of the mismatch-specific endonuclease method and denaturing high-performance liquid chromatography for the identification of HBB gene mutations. BMC Biotechnol 2008;8:62-70.
-
(2008)
BMC Biotechnol
, vol.8
, pp. 62-70
-
-
Hung, C.C.1
Su, Y.N.2
Lin, C.Y.3
Chang, Y.F.4
Chang, C.H.5
Cheng, W.F.6
-
26
-
-
17044426694
-
Advance in sequencing technology
-
Chan EY. Advance in sequencing technology. Mutat Res 2005;573:13-40.
-
(2005)
Mutat Res
, vol.573
, pp. 13-40
-
-
Chan, E.Y.1
-
27
-
-
34247844520
-
Application of diagnostic methods and molecular diagnosis of hemoglobin disorders in Khuzestan province of Iran
-
Fakher R, Bijan K, Taghi AM. Application of diagnostic methods and molecular diagnosis of hemoglobin disorders in Khuzestan province of Iran. Indian J Hum Genet 2007;13:5-15.
-
(2007)
Indian J Hum Genet
, vol.13
, pp. 5-15
-
-
Fakher, R.1
Bijan, K.2
Taghi, A.M.3
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