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Items: 1 to 20 of 579

1.

Modification of hemoglobin H disease by sickle trait.

Matthay KK, Mentzer WC Jr, Dozy AM, Kan YW, Bainton DF.

J Clin Invest. 1979 Oct;64(4):1024-32.

2.
3.

Sickle cell anemia associated with alpha-thalassemia in Malaysian Indians.

Lie-Injo LE, Hassan K, Joishy SK, Lim ML.

Am J Hematol. 1986 Jul;22(3):265-74.

PMID:
2424302
4.

The molecular basis of alpha-thalassemias: frequent occurrence of dysfunctional alpha loci among non-Asians with Hb H disease.

Orkin SH, Old J, Lazarus H, Altay C, Gurgey A, Weatherall DJ, Nathan DG.

Cell. 1979 May;17(1):33-42.

PMID:
455460
5.

Alpha thalassaemia in adults with sickle-cell trait.

Steinberg MH, Adams JG 3rd, Dreiling BJ.

Br J Haematol. 1975 May;30(1):31-7.

PMID:
1191571
6.

The effect of Hb F and alpha-thalassemia on the red cell indices in sickle cell anemia.

Milner PF, Garbutt GJ, Nolan-Davis LV, Jonah F, Wilson LB, Wilson JT.

Am J Hematol. 1986 Apr;21(4):383-95.

PMID:
2420172
7.

Gene mapping of Malaysian alpha thalassemias with alpha and zeta globin gene probes.

Lie-Injo LE, Herrera AR, Lebo RV, Hassan K, Lopez CG.

Am J Hematol. 1985 Mar;18(3):289-96.

PMID:
2983536
8.

Cord blood screening for alpha-thalassemia and hemoglobin variants by isoelectric focusing in northern Thai neonates: correlation with genotypes and hematologic parameters.

Charoenkwan P, Taweephol R, Sirichotiyakul S, Tantiprabha W, Sae-Tung R, Suanta S, Sakdasirisathaporn P, Sanguansermsri T.

Blood Cells Mol Dis. 2010 Jun 15;45(1):53-7. doi: 10.1016/j.bcmd.2010.02.015. Epub 2010 Mar 17.

PMID:
20299254
9.

The levels of zeta, gamma, and delta chains in patients with Hb H disease.

Kutlar F, Gonzalez-Redondo JM, Kutlar A, Gurgey A, Altay C, Efremov GD, Kleman K, Huisman TH.

Hum Genet. 1989 May;82(2):179-86.

PMID:
2566576
10.

Sickle cell syndromes. I. Hemoglobin SC-alpha-thalassemia.

Honig GR, Gunay U, Mason RG, Vida LN, Ferenc C.

Pediatr Res. 1976 Jun;10(6):613-20.

PMID:
1272638
11.

Effects of alpha-thalassemia-2 on the developmental changes of hematological values in children with sickle cell disease from Georgia.

Felice AE, McKie KM, Cleek MP, Marino EM, Kutlar A, McKie VC.

Am J Hematol. 1987 Aug;25(4):389-400.

PMID:
2441597
12.

Hb Bart's level in cord blood and deletions of alpha-globin genes.

Lie-Injo LE, Solai A, Herrera AR, Nicolaisen L, Kan YW, Wan WP, Hasan K.

Blood. 1982 Feb;59(2):370-6.

13.

Molecular analysis of Hb Q-H disease and Hb Q-Hb E in a Singaporean family.

Tan J, Tay JS, Wong YC, Kham SK, Bte Abd Aziz N, Teo SH, Wong HB.

Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:252-6.

PMID:
8629117
14.
15.

Longitudinal study of a newborn with a combination of deletion and nondeletion alpha-thalassemia-2.

Galanello R, Melis MA, Maccioni L, Pirastu M, Cao A.

Pediatr Res. 1984 Feb;18(2):158-62.

PMID:
6322098
17.

A new gene deletion involving the alpha 2-, alpha 1-, and theta 1-globin genes in a black family with Hb H disease.

Fei YJ, Liu JC, Walker EL 3rd, Huisman TH.

Am J Hematol. 1992 Apr;39(4):299-300.

PMID:
1553958
18.

Organization of alpha-chain genes among Hb G-Philadelphia heterozygotes in association with Hb S, beta-thalassemia, and alpha-thalassemia-2.

Felice AE, Ozdonmez R, Headlee ME, Huisman TH.

Biochem Genet. 1982 Aug;20(7-8):689-701. No abstract available.

PMID:
6291506
19.

[Hb Q-H: study of in vitro globin chain synthesis in reticulocytes and erythroblasts].

Beris P, Huber P, Spierer CL, Miescher PA.

Schweiz Med Wochenschr. 1986 Oct 25;116(43):1481-3. French.

PMID:
3787229
20.

Patterns of hemoglobin assembly in reticulocytes of sickle cell trait individuals.

Shaeffer JR, Longley MA, DeSimone J, Kleve LJ.

J Biol Chem. 1975 Nov 25;250(22):8630-4.

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