-
1
-
-
0028385688
-
1993 William Allan award address
-
Cao A 1994 1993 William Allan award address. Am J Hum Genet 54:397-402
-
(1994)
Am J Hum Genet
, vol.54
, pp. 397-402
-
-
Cao, A.1
-
3
-
-
0018248647
-
Thalassemia types and their incidence in Sardinia
-
Cao A, Galanello R, Furbetta M et al 1978 Thalassemia types and their incidence in Sardinia. J Med Genet 14:443-447
-
(1978)
J Med Genet
, vol.14
, pp. 443-447
-
-
Cao, A.1
Galanello, R.2
Furbetta, M.3
-
4
-
-
0019513029
-
Prevention of homozygous β-thalassemia by carrier screening and prenatal diagnosis in Sardinia
-
Cao A, Furbetta M, Galanello R et al 1981 Prevention of homozygous β-thalassemia by carrier screening and prenatal diagnosis in Sardinia. Am J Hum Genet 33:592-605
-
(1981)
Am J Hum Genet
, vol.33
, pp. 592-605
-
-
Cao, A.1
Furbetta, M.2
Galanello, R.3
-
5
-
-
0024404844
-
The prevention of thalassemia in Sardinia
-
Cao A, Rosatelli C, Galanello R et al 1989 The prevention of thalassemia in Sardinia. Clin Genet 36:277-285
-
(1989)
Clin Genet
, vol.36
, pp. 277-285
-
-
Cao, A.1
Rosatelli, C.2
Galanello, R.3
-
8
-
-
0024338661
-
Molecular analysis of β°-thalassemia intermedia in Sardinia
-
Galanello R, Dessì E, Melis MA et al 1989 Molecular analysis of β°-thalassemia intermedia in Sardinia. Blood 74:823-827
-
(1989)
Blood
, vol.74
, pp. 823-827
-
-
Galanello, R.1
Dessì, E.2
Melis, M.A.3
-
9
-
-
0025264871
-
Deletion δ-thalassemia: The 7.2kb deletion of Corfu δβ-thalassemia in a non-β-thalassemia chromosome
-
Galanello R, Melis MA, Podda A et al 1990 Deletion δ-thalassemia: the 7.2kb deletion of Corfu δβ-thalassemia in a non-β-thalassemia chromosome. Blood 75:1747-1748
-
(1990)
Blood
, vol.75
, pp. 1747-1748
-
-
Galanello, R.1
Melis, M.A.2
Podda, A.3
-
10
-
-
0028167553
-
A novel δ°-thalassemia mutation: TGG → TAG (Trp → STOP) at codon 37
-
Gasperini D, Perseu L, Cossu P et al 1994 A novel δ°-thalassemia mutation: TGG → TAG (Trp → STOP) at codon 37. Hum Mutat 3:71-72
-
(1994)
Hum Mutat
, vol.3
, pp. 71-72
-
-
Gasperini, D.1
Perseu, L.2
Cossu, P.3
-
11
-
-
0016744306
-
Prenatal diagnosis of homozygous β-thalassemia
-
Kan YW, Golbus MS, Trecartin RF et al 1975 Prenatal diagnosis of homozygous β-thalassemia. Lancet II:790-792
-
(1975)
Lancet
, vol.2
, pp. 790-792
-
-
Kan, Y.W.1
Golbus, M.S.2
Trecartin, R.F.3
-
12
-
-
0018919720
-
Polymorphism of DNA sequence in the β-globin gene region: Application to prenatal diagnosis of β° thalassemia in Sardinia
-
Kan YW, Lee KY, Furbetta M et al 1980 Polymorphism of DNA sequence in the β-globin gene region: application to prenatal diagnosis of β° thalassemia in Sardinia. N Engl J Med 302:185-188
-
(1980)
N Engl J Med
, vol.302
, pp. 185-188
-
-
Kan, Y.W.1
Lee, K.Y.2
Furbetta, M.3
-
13
-
-
0020580228
-
Phenotypic effect of heterozygous α- and β-thalassemia interaction
-
Melis MA, Pirastu M, Galanello R, Furbetta M, Tuveri T, Cao A 1983 Phenotypic effect of heterozygous α- and β-thalassemia interaction. Blood 62:226-229
-
(1983)
Blood
, vol.62
, pp. 226-229
-
-
Melis, M.A.1
Pirastu, M.2
Galanello, R.3
Furbetta, M.4
Tuveri, T.5
Cao, A.6
-
14
-
-
0024061172
-
Delineation of the molecular basis of δ and normal HbA2 β-thalassemia
-
Moi P, Paglietti E, Sanna A et al 1988 Delineation of the molecular basis of δ and normal HbA2 β-thalassemia. Blood 72:530-533
-
(1988)
Blood
, vol.72
, pp. 530-533
-
-
Moi, P.1
Paglietti, E.2
Sanna, A.3
-
15
-
-
0027195283
-
A promoter mutation of the β-globin gene (-101 C → T) has an age-related expression pattern
-
Murru S, Pirastu M, Sciarratta GV et al 1993 A promoter mutation of the β-globin gene (-101 C → T) has an age-related expression pattern. Blood 81:2818-2819
-
(1993)
Blood
, vol.81
, pp. 2818-2819
-
-
Murru, S.1
Pirastu, M.2
Sciarratta, G.V.3
-
16
-
-
0021870915
-
Genetic counselling and genetic heterogeneity in the thalassemias
-
Paglietti E, Galanello R, Addis M, Cao A 1985 Genetic counselling and genetic heterogeneity in the thalassemias. Clin Genet 28:1-7
-
(1985)
Clin Genet
, vol.28
, pp. 1-7
-
-
Paglietti, E.1
Galanello, R.2
Addis, M.3
Cao, A.4
-
17
-
-
0019944572
-
Alpha thalassemia in two Mediterranean populations
-
Pirastu M, Lee KY, Dozy AM et al 1982 Alpha thalassemia in two Mediterranean populations. Blood 60:509-512
-
(1982)
Blood
, vol.60
, pp. 509-512
-
-
Pirastu, M.1
Lee, K.Y.2
Dozy, A.M.3
-
19
-
-
0021355531
-
Multiple mutations produce δβ°-thalassemia in Sardinia
-
Pirastu M, Kan YW, Galanello R, Cao A 1984a Multiple mutations produce δβ°-thalassemia in Sardinia. Science 223:929-930
-
(1984)
Science
, vol.223
, pp. 929-930
-
-
Pirastu, M.1
Kan, Y.W.2
Galanello, R.3
Cao, A.4
-
20
-
-
0021747697
-
Initiation codon mutation as a cause of α thalassemia
-
Pirastu M, Saglio G, Chang JC et al 1984b Initiation codon mutation as a cause of α thalassemia. J Biol Chem 259:12315-12317
-
(1984)
J Biol Chem
, vol.259
, pp. 12315-12317
-
-
Pirastu, M.1
Saglio, G.2
Chang, J.C.3
-
21
-
-
0021254793
-
Hematological phenotype of the double heterozygous state for α- and β-thalassemia
-
Rosatelli MC, Falchi AM, Scalas MT et al 1984 Hematological phenotype of the double heterozygous state for α- and β-thalassemia. Hemoglobin 8:25-35
-
(1984)
Hemoglobin
, vol.8
, pp. 25-35
-
-
Rosatelli, M.C.1
Falchi, A.M.2
Scalas, M.T.3
-
22
-
-
84920234434
-
Prenatal diagnosis of beta thalassemia with the synthetic-oligomer technique
-
Rosatelli C, Falchi AM, Tuveri T et al 1985 Prenatal diagnosis of beta thalassemia with the synthetic-oligomer technique. Lancet 1:241-249
-
(1985)
Lancet
, vol.1
, pp. 241-249
-
-
Rosatelli, C.1
Falchi, A.M.2
Tuveri, T.3
-
23
-
-
0026556474
-
Molecular characterization of β-thalassemia in the Sardinian population
-
Rosatelli MC, Dozy A, Faà V et al 1992 Molecular characterization of β-thalassemia in the Sardinian population. Am J Hum Genet 50:422-426
-
(1992)
Am J Hum Genet
, vol.50
, pp. 422-426
-
-
Rosatelli, M.C.1
Dozy, A.2
Faà, V.3
-
24
-
-
0020424683
-
Hereditary anemias: Genetic basis, clinical features, diagnosis, and treatment
-
World Health Organization Working Group 1982 Hereditary anemias: genetic basis, clinical features, diagnosis, and treatment. Bull WHO 60:643-660
-
(1982)
Bull WHO
, vol.60
, pp. 643-660
-
-
|