-
1
-
-
0036190154
-
HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server
-
Hardison RC, Chui DHK, Giardine B, Riemer C, Patrinos GP, Anagnou N, Miller W, Wajcman H. HbVar: a relational database of human hemoglobin variants and thalassemia mutations at the globin gene server. Hum Mutat 2002;19(3):225-233 (http://globin.cse.psu.edu).
-
(2002)
Hum Mutat
, vol.19
, Issue.3
, pp. 225-233
-
-
Hardison, R.C.1
Chui, D.H.K.2
Giardine, B.3
Riemer, C.4
Patrinos, G.P.5
Anagnou, N.6
Miller, W.7
Wajcman, H.8
-
2
-
-
0347125141
-
-
Patrinos GP, Giardine B, Riemer C, Miller W, Chui DHK, Anagnou NP, Wajcman H, Hardison RC. Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies. Nucleic Acids Res 2004; 32(Database issue):D537-D541 (http://globin.cse.psu.edu).
-
Patrinos GP, Giardine B, Riemer C, Miller W, Chui DHK, Anagnou NP, Wajcman H, Hardison RC. Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies. Nucleic Acids Res 2004; 32(Database issue):D537-D541 (http://globin.cse.psu.edu).
-
-
-
-
3
-
-
0031886857
-
Molecular study and prenatal diagnosis of α- and β-thalassemias in Chinese
-
Ko TM, Xu X. Molecular study and prenatal diagnosis of α- and β-thalassemias in Chinese. J Formos Med Assoc 1998; 97(1):5-15.
-
(1998)
J Formos Med Assoc
, vol.97
, Issue.1
, pp. 5-15
-
-
Ko, T.M.1
Xu, X.2
-
4
-
-
0033784895
-
Molecular characterization and PCR detection of a deletional HPFH. Application to rapid prenatal diagnosis for compound heterozygotes of this defect with β-thalassemia in a Chinese family
-
Xu XM, Li ZQ, Liu ZY, Zhong XL, Zhao YZ, Mo QH. Molecular characterization and PCR detection of a deletional HPFH. Application to rapid prenatal diagnosis for compound heterozygotes of this defect with β-thalassemia in a Chinese family. Am J Hematol 2000; 65(3): 183-188.
-
(2000)
Am J Hematol
, vol.65
, Issue.3
, pp. 183-188
-
-
Xu, X.M.1
Li, Z.Q.2
Liu, Z.Y.3
Zhong, X.L.4
Zhao, Y.Z.5
Mo, Q.H.6
-
6
-
-
0031004892
-
Molecular characterization of β-thalassemia in Taiwan and the identification of two new mutations
-
Ko TM, Tseng LH, Hsu PM, Gun IJ, Lin YW, Li SF, Lee TY, Chuang SM. Molecular characterization of β-thalassemia in Taiwan and the identification of two new mutations. Hemoglobin 1997; 21(2):131-142.
-
(1997)
Hemoglobin
, vol.21
, Issue.2
, pp. 131-142
-
-
Ko, T.M.1
Tseng, L.H.2
Hsu, P.M.3
Gun, I.J.4
Lin, Y.W.5
Li, S.F.6
Lee, T.Y.7
Chuang, S.M.8
-
7
-
-
34247249951
-
Copy number analysis of survival motor neuron genes by multiplex ligation-dependent probe amplification
-
Huang CH, Chang YY, Chen CH, Kuo YS, Hwu WL, Gerdes T, Ko TM. Copy number analysis of survival motor neuron genes by multiplex ligation-dependent probe amplification. Genet Med 2007; 9(4):241-248.
-
(2007)
Genet Med
, vol.9
, Issue.4
, pp. 241-248
-
-
Huang, C.H.1
Chang, Y.Y.2
Chen, C.H.3
Kuo, Y.S.4
Hwu, W.L.5
Gerdes, T.6
Ko, T.M.7
-
13
-
-
0023391977
-
An approximately 300 bp deletion involving part of the 5′ β-globin gene region is observed in members of a Turkish family with β-thalassemia
-
Diaz-Chico JC, Yang KG, Kutlar A, Reese AL, Aksoy M, Huisman THJ. An approximately 300 bp deletion involving part of the 5′ β-globin gene region is observed in members of a Turkish family with β-thalassemia. Blood 1987; 70(2):583-586.
-
(1987)
Blood
, vol.70
, Issue.2
, pp. 583-586
-
-
Diaz-Chico, J.C.1
Yang, K.G.2
Kutlar, A.3
Reese, A.L.4
Aksoy, M.5
Huisman, T.H.J.6
-
14
-
-
0025228661
-
Human γ- to β-globin gene switching in transgenic mice
-
Behringer RR, Ryan TM, Palmiter RD, Brinster RL, Townes TM. Human γ- to β-globin gene switching in transgenic mice. Genes Dev 1990; 4(3):380-390.
-
(1990)
Genes Dev
, vol.4
, Issue.3
, pp. 380-390
-
-
Behringer, R.R.1
Ryan, T.M.2
Palmiter, R.D.3
Brinster, R.L.4
Townes, T.M.5
-
15
-
-
0025924718
-
0-thalassemia due to a 532-base pair deletion of the 5′ β-globin gene region
-
0-thalassemia due to a 532-base pair deletion of the 5′ β-globin gene region. Blood 1991; 77(5):1100-1103.
-
(1991)
Blood
, vol.77
, Issue.5
, pp. 1100-1103
-
-
Waye, J.S.1
Cai, S.P.2
Eng, B.3
Clark, C.4
Adams III, J.G.5
Chui, D.H.K.6
Steinberg, M.H.7
-
17
-
-
0022587268
-
Abnormal arrangements in the α- and γ-globin gene clusters in a relatively large group of Japanese newborns
-
Shimizu K, Harano T, Harano K, Miwa S, Amenomori Y, Ohba Y, Kutlar F, Huisman THJ. Abnormal arrangements in the α- and γ-globin gene clusters in a relatively large group of Japanese newborns. J Hum Genet 1986; 38(1):45-58.
-
(1986)
J Hum Genet
, vol.38
, Issue.1
, pp. 45-58
-
-
Shimizu, K.1
Harano, T.2
Harano, K.3
Miwa, S.4
Amenomori, Y.5
Ohba, Y.6
Kutlar, F.7
Huisman, T.H.J.8
-
18
-
-
0025992788
-
γ Chain abnormalities and γ-globin gene rearrangements in newborn babies of various populations
-
Huisman THJ, Kutlar F, Gu L-H. γ Chain abnormalities and γ-globin gene rearrangements in newborn babies of various populations. Hemoglobin 1991; 15(5):349-379.
-
(1991)
Hemoglobin
, vol.15
, Issue.5
, pp. 349-379
-
-
Huisman, T.H.J.1
Kutlar, F.2
Gu, L.-H.3
-
19
-
-
0032113846
-
Studies of fetal hemoglobin and γ-globin gene triplication in newborns in Jordan
-
Sadiq MF. Studies of fetal hemoglobin and γ-globin gene triplication in newborns in Jordan. Proc Natl Sci Counc Repub China B 1998; 22(3):108-113.
-
(1998)
Proc Natl Sci Counc Repub China B
, vol.22
, Issue.3
, pp. 108-113
-
-
Sadiq, M.F.1
|