-
1
-
-
0023753296
-
Determinations of the spectrum of β-thalassemia genes in Spain by use of dot-blot analysis of amplified β-gIobin DNA
-
Amselem. S., Nunes, V., Vidaud, M.. Estivill, X., Wong. C., d'Auriol. L, Vidaud, D., Galibert, E, Baiget, M. & Goosscns. M. (1988) Determinations of the spectrum of β-thalassemia genes in Spain by use of dot-blot analysis of amplified β-gIobin DNA. American Journal of Human Genetics, 43, 95-100.
-
(1988)
American Journal of Human Genetics
, vol.43
, pp. 95-100
-
-
Amselem, S.1
Nunes, V.2
Vidaud, M.3
Estivill, X.4
Wong, C.5
D'Auriol, L.6
Vidaud, D.7
Galibert, E.8
Baiget, M.9
Goosscns, M.10
-
2
-
-
0028447618
-
Anthropological approach to the heterogeneity of β-thalassemia mutations in Northern Africa
-
Bennani, C.,_Bouhass, R., Perrin-Pecontal. P., Tamouza, R., Malou, M.. Elion. j., Trabuchet. G.. Beldjord. C., Benabadji. M. & Labié. D. (1994) Anthropological approach to the heterogeneity of β-thalassemia mutations in Northern Africa. Human Biology. 66, 369-382.
-
(1994)
Human Biology.
, vol.66
, pp. 369-382
-
-
Bennani, C.1
Bouhass, R.2
Perrin-Pecontal, P.3
Tamouza, R.4
Malou, M.5
Elion, J.6
Trabuchet, G.7
Beldjord, C.8
Benabadji, M.9
Labié, D.10
-
3
-
-
0028792067
-
Prevention of ß-thalassemia major and Hb Bart's hydrops foetalis syndrome
-
Beris, P., Darbellay, R. & Exterman, P. (1995) Prevention of ß-thalassemia major and Hb Bart's hydrops foetalis syndrome. Seminars in Hematology. 32, 244-261.
-
(1995)
Seminars in Hematology.
, vol.32
, pp. 244-261
-
-
Beris, P.1
Darbellay, R.2
Exterman, P.3
-
4
-
-
36949068851
-
Estimation of small percentages of fetal haemoglobin
-
Betke, K., Marti. H.R. & Schlict. I. (1959) Estimation of small percentages of fetal haemoglobin. Nature, 184, 1877.
-
(1959)
Nature
, vol.184
, pp. 1877
-
-
Betke, K.1
Marti, H.R.2
Schlict, I.3
-
5
-
-
0024504090
-
/3-Thalassaemia mutations in Mediterranean population
-
Cao, A. (1989) /3-Thalassaemia mutations in Mediterranean population. British Journal of Haematologu, 71, 309-312.
-
(1989)
British Journal of Haematologu
, vol.71
, pp. 309-312
-
-
Cao, A.1
-
6
-
-
0023849720
-
The peculiar spectrum of j3-thalassemia genes in Tunisia
-
Chibani, J., Vidaud, M., Duquesnoy, P., Bergé-Lefranc, J.L., Pirastu, M., Ellouze, F., Rosa, J. & Goossens, M. (1988) The peculiar spectrum of j3-thalassemia genes in Tunisia. Human Genetics, 78, 190-192.
-
(1988)
Human Genetics
, vol.78
, pp. 190-192
-
-
Chibani, J.1
Vidaud, M.2
Duquesnoy, P.3
Bergé-Lefranc, J.L.4
Pirastu, M.5
Ellouze, F.6
Rosa, J.7
Goossens, M.8
-
7
-
-
0023849620
-
ThaIassemia mutations in the Portuguese population
-
Coutinho-Gomes, M.P., Gomes-da-Costa, M.G., Braga, L.B., CordeiroFerreira, N.T., Loi. A., Pirastu, M. & Cao. A. (1988) β-ThaIassemia mutations in the Portuguese population. Human Genetics. 78. 13-15.
-
(1988)
Human Genetics.
, vol.78
, pp. 13-15
-
-
Coutinho-Gomes, M.P.1
Gomes-da-Costa, M.G.2
Braga, L.B.3
Cordeiroferreira, N.T.4
Loi, A.5
Pirastu, M.6
Cao, A.7
-
8
-
-
0026767505
-
Novel promoter and splice Junctional defects add to the genetic, clinical or geographical heterogeneity of ß-thalassemia in the Portuguese population
-
Faustino, P., Osörio-AImeida, L., Barbot, J., Espîrito-Santo, D., Gonçalves, J., Romào, L, Martins, M.C., Marques, M.M. & Lavinha, J. (1992) Novel promoter and splice Junctional defects add to the genetic, clinical or geographical heterogeneity of ß-thalassemia in the Portuguese population. Human Genetics, 89, 573-576.
-
(1992)
Human Genetics
, vol.89
, pp. 573-576
-
-
Faustino, P.1
Osörio-Almeida, L.2
Barbot, J.3
Espîrito-Santo, D.4
Gonçalves, J.5
Romào, L.6
Martins, M.C.7
Marques, M.M.8
Lavinha, J.9
-
9
-
-
33847491299
-
The Haemoglobinopatliies: Techniques of Identification, Clinical and Biochemical Analysis, Vol. 6
-
Huisman, T.H.J. & Jonxis, J.H.P. (1977) The Haemoglobinopatliies: Techniques of Identification, Clinical and Biochemical Analysis, Vol. 6. Dekker, New York.
-
(1977)
Dekker, New York.
-
-
Huisman, T.H.J.1
Jonxis, J.H.P.2
-
10
-
-
0024457807
-
The molecular basis of ß-thalassemia in Bulgaria
-
Kalaydjieva, L., Eigel, A. & Horst, J. (1989) The molecular basis of ß-thalassemia in Bulgaria. Journal of Medical Genetics, 26, 614-618.
-
(1989)
Journal of Medical Genetics
, vol.26
, pp. 614-618
-
-
Kalaydjieva, L.1
Eigel, A.2
Horst, J.3
-
11
-
-
0023790820
-
Molecular basis and prenatal diagnosis of/3-thalassemia
-
Kazazian, H.H. & Boehm, C.D. (1988) Molecular basis and prenatal diagnosis of/3-thalassemia. Blood, 72, 1107-1116.
-
(1988)
Blood
, vol.72
, pp. 1107-1116
-
-
Kazazian, H.H.1
Boehm, C.D.2
-
12
-
-
0021399557
-
Molecular characterization of seven beta-thalassemia mutations in Asian Indians
-
Kazazian, H.H.. Jr. Orkin, S.H., Antonarakis, S.E., Sexton, J.P.. Boehm, C.D., Goff, S.C. & \Vaber, P.G. (1984a) Molecular characterization of seven beta-thalassemia mutations in Asian Indians. EMBO Journal, 3, 593-596.
-
(1984)
EMBO Journal
, vol.3
, pp. 593-596
-
-
Kazazian, H.H.1
Orkin Jr., S.H.2
Antonarakis, S.E.3
Sexton, J.P.4
Boehm, C.D.5
Goff, S.C.6
Vaber, P.G.7
-
13
-
-
0021252333
-
Quantification of the close association between DNA haplotypes and specific β-thaIassaemia mutations in Mediterranians
-
Kazazian. H.H... Jr, Orkin, S.H., Markham, A.F., Chapman, C.R., Youssoufian, H. & Waber, P.G. (1984b) Quantification of the close association between DNA haplotypes and specific β-thaIassaemia mutations in Mediterranians. Nature, 310, 152-154.
-
(1984)
Nature
, vol.310
, pp. 152-154
-
-
Kazazian Jr., H.H.1
Orkin, S.H.2
Markham, A.F.3
Chapman, C.R.4
Youssoufian, H.5
Waber, P.G.6
-
14
-
-
0027082932
-
Beta thalassemia in Spain and Portugal: Epidemiology and molecular pathology
-
Lavinha, J. & Baiget, M. (1992) Beta thalassemia in Spain and Portugal: epidemiology and molecular pathology. Hematology Reviews.6. 113-116.
-
(1992)
Hematology Reviews.
, vol.6
, pp. 113-116
-
-
Lavinha, J.1
Baiget, M.2
-
16
-
-
0025764288
-
Polymerase chain reaction (PCR) mutagenesis enabling rapid non-radioactive detection of common ß-thalassemia mutations in Mediterraneans
-
Lindeman, R., Hu, S.P., Volpato, F. & Trent, R.J. (1991) Polymerase chain reaction (PCR) mutagenesis enabling rapid non-radioactive detection of common ß-thalassemia mutations in Mediterraneans. British Journal of Haematologu, 78, 100-104.
-
(1991)
British Journal of Haematologu
, vol.78
, pp. 100-104
-
-
Lindeman, R.1
Hu, S.P.2
Volpato, F.3
Trent, R.J.4
-
17
-
-
0027479487
-
Hereditary anaemias in Portugal: Epidemiology, public health significance and control
-
Martins, M.C., Olim, G., Mélo, J., Magalhâes, H.A. & Rodrigues, M.O. (1993) Hereditary anaemias in Portugal: epidemiology, public health significance and control. Journal of Medical Genetics. 30, 235-239.
-
(1993)
Journal of Medical Genetics.
, vol.30
, pp. 235-239
-
-
Martins, M.C.1
Olim, G.2
Mélo, J.3
Magalhâes, H.A.4
Rodrigues, M.O.5
-
18
-
-
0028491884
-
Frequencia de las alteraciones moleculares de la ß-thalassemia hcterocigota en el sur de espana y su relacion con el fenötipo hematolögico
-
Molina, M.A., Romero, M.J.. Abril. E., Delgado, L, Cano, R.M., Garrido, F., Pablos, J.M. & Garrido. M.L. (1994) Frequencia de las alteraciones moleculares de la ß-thalassemia hcterocigota en el sur de espana y su relacion con el fenötipo hematolögico. Sangre, 39, 253-256.
-
(1994)
Sangre
, vol.39
, pp. 253-256
-
-
Molina, M.A.1
Romero, M.J.2
Abril, E.3
Delgado, L.4
Cano, R.M.5
Garrido, F.6
Pablos, J.M.7
Garrido, M.L.8
-
19
-
-
0025090540
-
Molecular characterization of j3-thalassemia mutations in Egypt
-
Novelette, A., Hafez, M., Deidda, G. Di-Rienzo, A., Felicetti, L., ElTahan, H., El-Morsi, Z., El-Ziny, M., Al-Tonbary, Y.. Sittien, A. & Terrenato, L. (1990) Molecular characterization of j3-thalassemia mutations in Egypt. Human Genetics. 85, 272-274.
-
(1990)
Human Genetics.
, vol.85
, pp. 272-274
-
-
Novelette, A.1
Hafez, M.2
Deidda, G.3
Di-Rienzo, A.4
Felicetti, L.5
Eltahan, H.6
El-Morsi, Z.7
El-Ziny, M.8
Al-Tonbary, Y.9
Sittien, A.10
Terrenato, L.11
-
20
-
-
0019949838
-
Linkage of 0-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster
-
Orkin, S.H., Kazazian, H.H.. Antonarakis, S.E., Golf, S.C., Boehm, CD.. Sexton, J.P.. Waber, P.C. & Giardina. P.J.V. (1982) Linkage of 0-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in 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
Golf, S.C.4
Boehm, C.D.5
Sexton, J.P.6
Waber, P.C.7
Giardina, P.J.V.8
-
21
-
-
0023689331
-
DNA haplotype distribution in Algerian β-thalassemia patients: An extended evaluation by family studies and representative molecular characterization
-
Rouabhi, L., Lapoumeroulie, C., Amselcm, S., Krishnamoorthy, R.. Adjrad, L., Girot, R., Chardin, P., Benabdji, M.. Labié. D. & Beldjord, C. (1988) DNA haplotype distribution in Algerian β-thalassemia patients: an extended evaluation by family studies and representative molecular characterization. Human Genetics, 79, 373-376.
-
(1988)
Human Genetics
, vol.79
, pp. 373-376
-
-
Rouabhi, L.1
Lapoumeroulie, C.2
Amselcm, S.3
Krishnamoorthy, R.4
Adjrad, L.5
Girot, R.6
Chardin, P.7
Benabdji, M.8
Labié, D.9
Beldjord, C.10
-
22
-
-
0024558230
-
A j3thalassemia gene caused by a 290 base pair deletion: Analysis by direct sequencing of enzymatically amplified DNA
-
Spielberg. R., Aulehla-Scholz, C.. Erlich, H. & Horst, J. (1989) A j3thalassemia gene caused by a 290 base pair deletion: analysis by direct sequencing of enzymatically amplified DNA. Blood, 73, 1695-1698.
-
(1989)
Blood
, vol.73
, pp. 1695-1698
-
-
Spielberg, R.1
Aulehla-Scholz, C.2
Erlich, H.3
Horst, J.4
-
23
-
-
0027524125
-
Beta-thalassemia mutations in he Portuguese: High frequencies of two alleles in restricted populations
-
Tamagnini, G.P., Gonçalves, P., Ribeiro, M.L.S., Kaeda, J., Kutlar, F., Baysal, E. & Huisman, T.H.J. (1993) Beta-thalassemia mutations in (he Portuguese: high frequencies of two alleles in restricted populations. Hemoglobin, 17, 31-40.
-
(1993)
Hemoglobin
, vol.17
, pp. 31-40
-
-
Tamagnini, G.P.1
Gonçalves, P.2
Ribeiro, M.L.S.3
Kaeda, J.4
Kutlar, F.5
Baysal, E.6
Huisman, T.H.J.7
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