-
1
-
-
0013935942
-
Abnormal human hemoglobins. Separation and characterization of the α- And β-chains by chromatography and the determination of two new variants, Hb Chesapeake and Hb J (Bangkok)
-
Clegg, J.B., Naughton, M.A. and Weatherall, D.J. (1966) Abnormal human hemoglobins. Separation and characterization of the α- and β-chains by chromatography and the determination of two new variants, Hb Chesapeake and Hb J (Bangkok). J. Mol. Biol., 19, 91-96.
-
(1966)
J. Mol. Biol.
, vol.19
, pp. 91-96
-
-
Clegg, J.B.1
Naughton, M.A.2
Weatherall, D.J.3
-
2
-
-
0028214609
-
Rapid detection of deletions causing δβ-thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification
-
Craig, J.E., Barnetson, R.A., Prior, J. et al. (1994) Rapid detection of deletions causing δβ-thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification. Blood, 83, 1673-1682.
-
(1994)
Blood
, vol.83
, pp. 1673-1682
-
-
Craig, J.E.1
Barnetson, R.A.2
Prior, J.3
-
3
-
-
0025358932
-
Rapid detection of hypervariable regions by the polymerase chain reaction technique
-
Decorte, R., Cuppens, H., Marynen, P. et al. (1990) Rapid detection of hypervariable regions by the polymerase chain reaction technique. DNA Cell Biol., 9, 461-469.
-
(1990)
DNA Cell Biol.
, vol.9
, pp. 461-469
-
-
Decorte, R.1
Cuppens, H.2
Marynen, P.3
-
4
-
-
0029038302
-
Allelic drop-out and preferential amplification in single cells and human blastomeres for preimplantation diagnosis of sex and cystic fibrosis
-
Findlay, I., Ray, P., Quirke, P. et al. (1995) Allelic drop-out and preferential amplification in single cells and human blastomeres for preimplantation diagnosis of sex and cystic fibrosis. Hum. Reprod., 10, 1609-1618.
-
(1995)
Hum. Reprod.
, vol.10
, pp. 1609-1618
-
-
Findlay, I.1
Ray, P.2
Quirke, P.3
-
5
-
-
0030051512
-
Limb defects and chorionic villus sampling: Results from an international registry, 1992-94
-
Froster, U.G. and Jackson, L. (1996) Limb defects and chorionic villus sampling: results from an international registry, 1992-94. Lancet, 347, 489-494.
-
(1996)
Lancet
, vol.347
, pp. 489-494
-
-
Froster, U.G.1
Jackson, L.2
-
6
-
-
0025264871
-
Deletion δ-thalassemia: The 7.2kb deletion of Corfu δβ-thalassemia in a non-β-thalassemia chromosome
-
Galanello, R., Melis, M.A., Podda, A. et al. (1990) Deletion δ-thalassemia: the 7.2kb deletion of Corfu δβ-thalassemia in a non-β-thalassemia chromosome. Blood, 75, 1747-1749.
-
(1990)
Blood
, vol.75
, pp. 1747-1749
-
-
Galanello, R.1
Melis, M.A.2
Podda, A.3
-
7
-
-
0007758208
-
Polymorphisms of DNA sequence adjacent to human β-globin structural gene: Relation to sickle mutation
-
Kan, Y.W. and Dozy, A.M. (1978) Polymorphisms of DNA sequence adjacent to human β-globin structural gene: relation to sickle mutation. Proc. Natl. Acad. Sci. USA, 75, 5631-5635.
-
(1978)
Proc. Natl. Acad. Sci. USA
, vol.75
, pp. 5631-5635
-
-
Kan, Y.W.1
Dozy, A.M.2
-
8
-
-
0017139208
-
Prenatal diagnosis of α-thalassemia: Clinical application of molecular hybridization
-
Kan, Y.W., Globus, M.S. and Dozy, A.M. (1976) Prenatal diagnosis of α-thalassemia: clinical application of molecular hybridization. N. Engl. J. Med., 295, 1161-1169.
-
(1976)
N. Engl. J. Med.
, vol.295
, pp. 1161-1169
-
-
Kan, Y.W.1
Globus, M.S.2
Dozy, A.M.3
-
9
-
-
0022456383
-
Frequency of α-thalassemia in Greece
-
Kanavakis, E., Tzotzos, S., Liapaki, A. et al. (1986) Frequency of α-thalassemia in Greece. Am. J. Hematol., 22, 225-232.
-
(1986)
Am. J. Hematol.
, vol.22
, pp. 225-232
-
-
Kanavakis, E.1
Tzotzos, S.2
Liapaki, A.3
-
10
-
-
0025220340
-
Molecular characterization of β-thalassemia in 174 Greek patients with thataisemia major
-
Kattamis, C., Hu, H., Cheng, G. et al. (1990) Molecular characterization of β-thalassemia in 174 Greek patients with thataisemia major. Br. J. Haematol., 74, 342-346.
-
(1990)
Br. J. Haematol.
, vol.74
, pp. 342-346
-
-
Kattamis, C.1
Hu, H.2
Cheng, G.3
-
11
-
-
85016800269
-
Use of PCR in the diagnosis of monogenic diseases
-
Erlich, H.A. (ed.), Stockton Press, New York
-
Kazazian, H.H (1989) Use of PCR in the diagnosis of monogenic diseases. In Erlich, H.A. (ed.), PCR Technology. Stockton Press, New York, pp. 153-169.
-
(1989)
PCR Technology
, pp. 153-169
-
-
Kazazian, H.H.1
-
12
-
-
0025197914
-
Denaturing gradient gel electrophoresis and direct sequencing of PCR amplified genomic DNA: A rapid and reliable diagnostic approach to beta thalassemia
-
Losekoot, M., Fodde, R., Harteveld, C.L. et al. (1990) Denaturing gradient gel electrophoresis and direct sequencing of PCR amplified genomic DNA: a rapid and reliable diagnostic approach to beta thalassemia. Br. J. Haematol., 76, 269-274.
-
(1990)
Br. J. Haematol.
, vol.76
, pp. 269-274
-
-
Losekoot, M.1
Fodde, R.2
Harteveld, C.L.3
-
13
-
-
0026779977
-
Multiplex PCR amplification of three microsatellites within the CFTR gene
-
Morral, N. and Estivill, X. (1992) Multiplex PCR amplification of three microsatellites within the CFTR gene. Genomics, 13, 1362-1364.
-
(1992)
Genomics
, vol.13
, pp. 1362-1364
-
-
Morral, N.1
Estivill, X.2
-
14
-
-
0022965004
-
-
Mullis, K.B., Faloona, F., Scharf, S.J. et al. (1986) Cold Spring Harbor Symp. Quant. Biol., 51, 263-273.
-
(1986)
Cold Spring Harbor Symp. Quant. Biol.
, vol.51
, pp. 263-273
-
-
Mullis, K.B.1
Faloona, F.2
Scharf, S.J.3
-
15
-
-
0002804385
-
Gene analysis
-
Weatherall, D.J. (ed.), Churchill Livingstone, London
-
Old, J.M. and Higgs, D.R. (1982) Gene analysis. In Weatherall, D.J. (ed.), Methods in Haematology: The Thalassaemias. Churchill Livingstone, London, pp. 74-102.
-
(1982)
Methods in Haematology: The Thalassaemias
, pp. 74-102
-
-
Old, J.M.1
Higgs, D.R.2
-
16
-
-
0025090944
-
Rapid detection and prenatal diagnosis of β-thalassaemia: Studies in Indian and Cypriot populations in the UK
-
Old, J.M., Varawalla, N.Y. and Weatherall, D.J. (1990) Rapid detection and prenatal diagnosis of β-thalassaemia: studies in Indian and Cypriot populations in the UK. Lancet, 33, 834-837.
-
(1990)
Lancet
, vol.33
, pp. 834-837
-
-
Old, J.M.1
Varawalla, N.Y.2
Weatherall, D.J.3
-
17
-
-
0018099170
-
Application of endonuclease mapping to the analysis and prenatal diagnosis of thalassemia caused by globin-gene deletion
-
Orkin, S.H., Alter, B.P., Altay, C. et al. (1978) Application of endonuclease mapping to the analysis and prenatal diagnosis of thalassemia caused by globin-gene deletion. N. Engl. J. Med., 299, 166-170.
-
(1978)
N. Engl. J. Med.
, vol.299
, pp. 166-170
-
-
Orkin, S.H.1
Alter, B.P.2
Altay, C.3
-
18
-
-
0019949838
-
Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in the human β-globin gene cluster
-
Orkin, S.H., Kazazian, H.H., Antonarakis, S.E. et al. (1982) Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in the human β-globin gene cluster Nature, 296, 627-631.
-
(1982)
Nature
, vol.296
, pp. 627-631
-
-
Orkin, S.H.1
Kazazian, H.H.2
Antonarakis, S.E.3
-
19
-
-
0024376665
-
Polymerase chain reaction applied to the determination of β-like globin gene cluster haplotypes
-
Sutton, M., Bouhassira, E.E. and Nagel, R.L. (1989) Polymerase chain reaction applied to the determination of β-like globin gene cluster haplotypes. Am. J. Hematol., 32, 66-69.
-
(1989)
Am. J. Hematol.
, vol.32
, pp. 66-69
-
-
Sutton, M.1
Bouhassira, E.E.2
Nagel, R.L.3
-
20
-
-
0028097269
-
Recycling the single cell to detect specific chromosomes and to investigate specific gene sequences
-
Thornhill, A., Holding, C. and Monk, M. (1994) Recycling the single cell to detect specific chromosomes and to investigate specific gene sequences. Hum. Reprod., 9, 2150-2155.
-
(1994)
Hum. Reprod.
, vol.9
, pp. 2150-2155
-
-
Thornhill, A.1
Holding, C.2
Monk, M.3
-
21
-
-
0027431221
-
Characterization of nondeletion α-thalassemia mutations in the Greek population
-
Traeger-Synodinos, J., Kanavakis, E., Tzetis, M. et al. (1993) Characterization of nondeletion α-thalassemia mutations in the Greek population. Am. J. Hematol., 44, 162-167.
-
(1993)
Am. J. Hematol.
, vol.44
, pp. 162-167
-
-
Traeger-Synodinos, J.1
Kanavakis, E.2
Tzetis, M.3
-
22
-
-
24544453870
-
Rare β-thalassemia alleles in the Greek and Greek Cypriot populations
-
Traeger-Synodinos, J., Maragoudaki, E., Vrettou, C. et al. (1996) Rare β-thalassemia alleles in the Greek and Greek Cypriot populations. Br. J. Haematol., 93 (Suppl. 2), 100A.
-
(1996)
Br. J. Haematol.
, vol.93
, Issue.2 SUPPL.
-
-
Traeger-Synodinos, J.1
Maragoudaki, E.2
Vrettou, C.3
-
23
-
-
0028226417
-
The molecular basis of normal HbA2 (type 2) β-thalassemia in Greece
-
Tzetis, M., Traeger-Synodinos, J., Kanavakis, E. et al. (1994) The molecular basis of normal HbA2 (type 2) β-thalassemia in Greece. Hematologic Pathology, 8, 25-34.
-
(1994)
Hematologic Pathology
, vol.8
, pp. 25-34
-
-
Tzetis, M.1
Traeger-Synodinos, J.2
Kanavakis, E.3
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