Similar articles for PMID: 4030382

Year	Number of Results
1965	2
1966	3
1967	5
1968	1
1970	2
1972	2
1973	2
1974	1
1975	3
1976	3
1977	1
1978	5
1979	6
1980	4
1981	7
1982	8
1983	7
1984	8
1985	10
1986	8
1987	6
1988	7
1989	5
1990	4
1991	4
1992	3
1993	1
1994	1
1995	1
1997	1
1998	2
1999	2
2000	1
2002	2
2004	2
2006	1
2008	1
2009	1
2012	1
2013	4
2014	1
2016	2
2017	2
2020	4
2021	2
2024	0

1

Hemoglobin Cocody [beta 21 (B3)Asp----Asn] hematologic aspects of heterozygosity and of Hb Cocody/beta +-thalassemia.

Fabritius H, Cabannes R, Boissel JP, Wacjman H, Labie D. Fabritius H, et al. Hemoglobin. 1985;9(2):193-6. doi: 10.3109/03630268508997003. Hemoglobin. 1985. PMID: 4030382 No abstract available.

2

Modification of hemoglobin H disease by sickle trait.

Matthay KK, Mentzer WC Jr, Dozy AM, Kan YW, Bainton DF. Matthay KK, et al. J Clin Invest. 1979 Oct;64(4):1024-32. doi: 10.1172/JCI109539. J Clin Invest. 1979. PMID: 479366 Free PMC article.

3

[Hematologic characterization and analysis of genetic transmission in a case of double heterozygosity Hb Lepore/beta-thalassemia].

De Caterina M, Esposito P, Remondelli P, Esposito S. De Caterina M, et al. Quad Sclavo Diagn. 1985 Dec;21(4):412-8. Quad Sclavo Diagn. 1985. PMID: 3837915 Italian.

4

HB S-HB Monroe; a sickle cell-beta-thalassemia syndrome.

Sweeting I, Serjeant BE, Serjeant GR, Kulozik AE, Vetter B. Sweeting I, et al. Hemoglobin. 1998 Mar;22(2):153-6. doi: 10.3109/03630269809092139. Hemoglobin. 1998. PMID: 9576332 No abstract available.

5

Hemoglobin Setif and in vitro pseudosickling noted in a family with co-existent alpha and beta thalassemia.

Raik E, Powell E, Fleming P, Gordon S. Raik E, et al. Pathology. 1983 Oct;15(4):453-6. doi: 10.3109/00313028309085174. Pathology. 1983. PMID: 6674875

6

Hb Cocody [beta 21(B3)Asp----Asn] and Hb Yusa [beta 21(B3)ASP----TYR] found in Japan.

Ohba Y, Hattori Y, Ami Y, Yagami H, Miyaji T, Tani Y. Ohba Y, et al. Hemoglobin. 1990;14(1):109-14. doi: 10.3109/03630269009002259. Hemoglobin. 1990. PMID: 2384310 No abstract available.

7

Two new cases of heterozygosity for hemoglobin Knossos alpha 2 beta 2 27 Ala----Ser detected in the French West Indies and Algeria.

Galacteros F, Garin JD, Monplaisir N, Namoune S, Arous N, Blouquit Y, Mamalaki A, Tulliez M, Ouka M, Goossens M, et al. Galacteros F, et al. Hemoglobin. 1984;8(3):215-28. doi: 10.3109/03630268408996970. Hemoglobin. 1984. PMID: 6469698

8

Hemoglobin New York associated with alpha-thalassemia.

Kendall A, Pang W. Kendall A, et al. Hum Hered. 1980;30(1):50-3. doi: 10.1159/000153089. Hum Hered. 1980. PMID: 7353889

9

[Double heterozygote hemoglobin D/B0 thalassemia. Report of 3 cases in a Portuguese family].

Sousa Uva L, Fernandes A, Pilar M. Sousa Uva L, et al. Nouv Rev Fr Hematol (1978). 1983;25(6):387-90. Nouv Rev Fr Hematol (1978). 1983. PMID: 6664837 French.

10

Silent beta-thalassemia associated with Hb Knossos beta 27 (B9) Ala replaced by Ser in Algeria.

Rouabhi F, Chardin P, Boissel JP, Beghoul F, Labie D, Benabadji M. Rouabhi F, et al. Hemoglobin. 1983;7(6):555-61. doi: 10.3109/03630268309027935. Hemoglobin. 1983. PMID: 6668188 No abstract available.

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