-
1
-
-
0025641081
-
0-thalassemia in a Sicilian family
-
0-thalassemia in a Sicilian family. Hemoglobin 1990; 14(5):549-553.
-
(1990)
Hemoglobin
, vol.14
, Issue.5
, pp. 549-553
-
-
Corso, D.1
Cognata, B.2
Ciaccio, C.3
Piazza, T.4
Dibenedetto, S.P.5
Samperi, P.6
Russo Mancuso, G.7
Schiliro, G.8
-
2
-
-
0023696177
-
Hemoglobin Agenogi in Hungary
-
Földi J, Horányi M, Szelényi JG, Hollán SR, Kiss A, Spivak VA, Aseeva EA, Tasheva ES, Tokarev YuN. Hemoglobin Agenogi in Hungary. Hemoglobin 1988; 12(3):395-398.
-
(1988)
Hemoglobin
, vol.12
, Issue.3
, pp. 395-398
-
-
Földi, J.1
Horányi, M.2
Szelényi, J.G.3
Hollán, S.R.4
Kiss, A.5
Spivak, V.A.6
Aseeva, E.A.7
Tasheva, E.S.8
Tokarev, Yu.N.9
-
3
-
-
0020754948
-
A case of Hemoglobin Agenogi in a Sicilian family
-
Minafra S, D'Antoni S, Russo G, Bosco E, Marinucci M, Pucci E. A case of Hemoglobin Agenogi in a Sicilian family. Haematologica 1983; 68(3):320-327.
-
(1983)
Haematologica
, vol.68
, Issue.3
, pp. 320-327
-
-
Minafra, S.1
D'Antoni, S.2
Russo, G.3
Bosco, E.4
Marinucci, M.5
Pucci, E.6
-
4
-
-
0013966414
-
2β2 90 Lys), a slow-moving hemoglobin of a Japanese family resembling Hb-E
-
2β2 90 Lys), a slow-moving hemoglobin of a Japanese family resembling Hb-E. Clin Chim Acta 1966; 14(5):624-629.
-
(1966)
Clin Chim Acta
, vol.14
, Issue.5
, pp. 624-629
-
-
Miyaji, T.1
Suzuki, H.2
Ohba, Y.3
Shibata, S.4
-
5
-
-
0036065710
-
Hb Agenogi [β90(F6)Glu→Lys] in an Argentinean girl
-
Noguera NI, Cardozo MA, González FA, Benavente C, Milani AC, Villegas A. Hb Agenogi [β90(F6)Glu→Lys] in an Argentinean girl. Hemoglobin 2002; 26(2):201-203.
-
(2002)
Hemoglobin
, vol.26
, Issue.2
, pp. 201-203
-
-
Noguera, N.I.1
Cardozo, M.A.2
González, F.A.3
Benavente, C.4
Milani, A.C.5
Villegas, A.6
-
6
-
-
0032160450
-
Hemoglobin Agenogi [β90(F6)Glu→Lys] found in Piedmont. Case report
-
Scime-Degani V, Ivaldi G, David O, De Paola M, Rabino-Massa E, Ricco G. Hemoglobin Agenogi [β90(F6)Glu→Lys] found in Piedmont. Case report. Panminerva Med 1998; 40(3):250-253.
-
(1998)
Panminerva Med
, vol.40
, Issue.3
, pp. 250-253
-
-
Scime-Degani, V.1
Ivaldi, G.2
David, O.3
De Paola, M.4
Rabino-Massa, E.5
Ricco, G.6
-
7
-
-
0010114289
-
Hemoglobin S Antilles: A variant with lower solubility than Hemoglobin S and producing sickle cell disease in heterozygotes
-
Monplaisir N, Merault G, Poyart C, Rhoda MD, Craescu C, Vidaud M, Galacteros F, Blouquit Y, Rosa J. Hemoglobin S Antilles: a variant with lower solubility than Hemoglobin S and producing sickle cell disease in heterozygotes. Proc Natl Acad Sci U S A 1986; 83(24):9363-9367.
-
(1986)
Proc Natl Acad Sci U S A
, vol.83
, Issue.24
, pp. 9363-9367
-
-
Monplaisir, N.1
Merault, G.2
Poyart, C.3
Rhoda, M.D.4
Craescu, C.5
Vidaud, M.6
Galacteros, F.7
Blouquit, Y.8
Rosa, J.9
-
8
-
-
0023720269
-
Hb A-like sickle haemoglobin: Hb S-Providence
-
Gale RE, Blair NE, Huehns ER, Clegg JB. Hb A-like sickle haemoglobin: Hb S-Providence. Br J Haematol 1988; 70(2):251-252.
-
(1988)
Br J Haematol
, vol.70
, Issue.2
, pp. 251-252
-
-
Gale, R.E.1
Blair, N.E.2
Huehns, E.R.3
Clegg, J.B.4
-
9
-
-
0024632641
-
Case report - A new doubly substituted sickling haemoglobin: Hb S-Oman
-
Langdown JV, Williamson D, Knight CB, Rubenstein D, Carrell RW. Case report - a new doubly substituted sickling haemoglobin: Hb S-Oman. Br J Haematol 1989; 71(3):443-444.
-
(1989)
Br J Haematol
, vol.71
, Issue.3
, pp. 443-444
-
-
Langdown, J.V.1
Williamson, D.2
Knight, C.B.3
Rubenstein, D.4
Carrell, R.W.5
-
10
-
-
0032400879
-
Hb S-Oman heterozygote: A new dominant sickle syndrome
-
Nagel RL, Daar S, Romero JR, Suzuka SM, Gravell D, Bouhassira E, Schwartz RS, Fabry ME, Krishnamoorthy R. Hb S-Oman heterozygote: a new dominant sickle syndrome. Blood 1998; 92(11):4375-4382.
-
(1998)
Blood
, vol.92
, Issue.11
, pp. 4375-4382
-
-
Nagel, R.L.1
Daar, S.2
Romero, J.R.3
Suzuka, S.M.4
Gravell, D.5
Bouhassira, E.6
Schwartz, R.S.7
Fabry, M.E.8
Krishnamoorthy, R.9
-
11
-
-
0017412345
-
Hemoglobin S Travis: A sickling hemoglobin with two amino acid substitutions [β6(A3)Glu→Val and (142(H20)Ala→Val]
-
Moo-Penn WF, Schmidt RM, Jue DL, Bechtel KC, Wright JM, Horne MK III, Haycraft GL, Roth EF Jr, Nagel RL. Hemoglobin S Travis: a sickling hemoglobin with two amino acid substitutions [β6(A3)Glu→Val and (142(H20)Ala→Val]. Eur J Biochem 1977; 77(3):561-566.
-
(1977)
Eur J Biochem
, vol.77
, Issue.3
, pp. 561-566
-
-
Moo-Penn, W.F.1
Schmidt, R.M.2
Jue, D.L.3
Bechtel, K.C.4
Wright, J.M.5
Horne III, M.K.6
Haycraft, G.L.7
Roth Jr., E.F.8
Nagel, R.L.9
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