-
1
-
-
0023796168
-
Counselling for prenatal diagnosis of sickle cell disease and β thalassemia major: A four year experience
-
ANIONWU E.N., PATEL N., KANJI G., RENGES H. and BROZOVIC M.: Counselling for prenatal diagnosis of sickle cell disease and β thalassemia major: a four year experience. J. Med. Genet., 1988, 25, 769-772.
-
(1988)
J. Med. Genet.
, vol.25
, pp. 769-772
-
-
Anionwu, E.N.1
Patel, N.2
Kanji, G.3
Renges, H.4
Brozovic, M.5
-
2
-
-
0025275664
-
Factors influencing the reproductive decision after genetic counseling
-
FRETS P.G., DUIVENVOORDEN H.J. and VERHAGE F., et al.: Factors influencing the reproductive decision after genetic counseling. Am. J. Med. Genet., 1990, 35, 496-502.
-
(1990)
Am. J. Med. Genet.
, vol.35
, pp. 496-502
-
-
Frets, P.G.1
Duivenvoorden, H.J.2
Verhage, F.3
-
3
-
-
0024446352
-
Mortality in children and adolescents with sickle cell disease
-
LEIKIN S.L., GALLAGHER D. and KINNEY T R., et al.: Mortality in children and adolescents with sickle cell disease. Pediatrics, 1989, 84, 500-508.
-
(1989)
Pediatrics
, vol.84
, pp. 500-508
-
-
Leikin, S.L.1
Gallagher, D.2
Kinney, T.R.3
-
4
-
-
0026316541
-
Prenatal Hemoglobinopathy Screening. IV. Follow-up of women at risk for a child with a clinically significant hemoglobinopathy
-
LOADER S., SUTERA C.J., SEGELMAN S.G., KOZYRA A. and ROWLEY P.T.: Prenatal Hemoglobinopathy Screening. IV. Follow-up of women at risk for a child with a clinically significant hemoglobinopathy. Am. J. Hum. Genet., 1991, 49, 1292-1299.
-
(1991)
Am. J. Hum. Genet.
, vol.49
, pp. 1292-1299
-
-
Loader, S.1
Sutera, C.J.2
Segelman, S.G.3
Kozyra, A.4
Rowley, P.T.5
-
5
-
-
0027517308
-
β-globin gene cluster haplotype and α-thalassemia do not correlate with the acute clinical manifestations of sickle cell disease in children
-
DE MONTALEMBERT M., MAIERREDELSPERGER M. and GIROT R., et al.: β-globin gene cluster haplotype and α-thalassemia do not correlate with the acute clinical manifestations of sickle cell disease in children. Blood, 1993, 82, 2595-2596.
-
(1993)
Blood
, vol.82
, pp. 2595-2596
-
-
De Montalembert, M.1
Maierredelsperger, M.2
Girot, R.3
-
6
-
-
0027363440
-
Epidemiological and clinical study of sickle cell disease in France, French Guiana and Algeria
-
DE MONTALEMBERT M., GUILLOUDBATAILLE M., FEINGOLD J. and GIROT R.: Epidemiological and clinical study of sickle cell disease in France, French Guiana and Algeria. Eur. J. Haematol., 1993, 51, 136-140.
-
(1993)
Eur. J. Haematol.
, vol.51
, pp. 136-140
-
-
De Montalembert, M.1
Guilloudbataille, M.2
Feingold, J.3
Girot, R.4
-
7
-
-
0026484251
-
Factors affecting the uptake of prenatal diagnosis for sickle cell disease
-
PETROU M., BRUGIATELLI M., WARD R.H.T. and MODELL B.: Factors affecting the uptake of prenatal diagnosis for sickle cell disease. J. Med. Genet., 1992, 29, 820-823.
-
(1992)
J. Med. Genet.
, vol.29
, pp. 820-823
-
-
Petrou, M.1
Brugiatelli, M.2
Ward, R.H.T.3
Modell, B.4
-
8
-
-
0028291736
-
Mortality in sickle cell disease. Life expectancy and risk factors for early death
-
PLATT O.S., BRAMBILLA D.J. and ROSSE WF., et al.: Mortality in sickle cell disease. Life expectancy and risk factors for early death. Blood. 1994, 330, 1639-1644.
-
(1994)
Blood
, vol.330
, pp. 1639-1644
-
-
Platt, O.S.1
Brambilla, D.J.2
Rosse, W.F.3
-
9
-
-
0025569563
-
Sickle cell anemia and major organ failure
-
POWARS D.: Sickle cell anemia and major organ failure. Hemoglobin., 1990, 14, 573-598.
-
(1990)
Hemoglobin
, vol.14
, pp. 573-598
-
-
Powars, D.1
-
10
-
-
0027370957
-
Diagnosis of sickle-cell disease with an universal heteroduplex generator
-
WOOD N., STANDEN G., HOWS J., BRADLEY B. and BIDWELL J.: Diagnosis of sickle-cell disease with an universal heteroduplex generator Lancet, 1993, 342, 1519-1520.
-
(1993)
Lancet
, vol.342
, pp. 1519-1520
-
-
Wood, N.1
Standen, G.2
Hows, J.3
Bradley, B.4
Bidwell, J.5
|