Coleman M - Search Results

1

Dominant thalassemia-like phenotypes associated with mutations in exon 3 of the beta-globin gene.

Kazazian HH Jr, Dowling CE, Hurwitz RL, Coleman M, Stopeck A, Adams JG 3rd. Kazazian HH Jr, et al. Among authors: coleman m. Blood. 1992 Jun 1;79(11):3014-8. Blood. 1992. PMID: 1586746 Free article.

2

A four-base deletion 5' to the A gamma globin gene is a common polymorphism.

Coleman MB, Steinberg MH, Adams JG 3rd. Coleman MB, et al. Blood. 1991 Nov 1;78(9):2473-4. Blood. 1991. PMID: 1681964 Free article. No abstract available.

3

Molecular basis for alpha-thalassemia associated with the structural mutant hemoglobin Suan-Dok (alpha 2 109leu----arg).

Weiss I, Cash FE, Coleman MB, Pressley A, Adams JG, Sanguansermsri T, Liebhaber SA, Steinberg MH. Weiss I, et al. Among authors: coleman mb. Blood. 1990 Dec 15;76(12):2630-6. Blood. 1990. PMID: 2265255 Free article.

4

A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(--/alpha alpha) in blacks: HbH disease in sickle cell trait.

Steinberg MH, Coleman MB, Adams JG 3rd, Hartmann RC, Saba H, Anagnou NP. Steinberg MH, et al. Among authors: coleman mb. Blood. 1986 Feb;67(2):469-73. Blood. 1986. PMID: 3942832 Free article.

5

Beta-thalassemia with exceptionally high hemoglobin A2. Differential expression of the delta-globin gene in the presence of beta-thalassemia.

Steinberg MH, Coleman MB, Adams JG 3rd. Steinberg MH, et al. Among authors: coleman mb. J Lab Clin Med. 1982 Oct;100(4):548-57. J Lab Clin Med. 1982. PMID: 6288819

6

Effects of thalassemia and microcytosis on the hematologic and vasoocclusive severity of sickle cell anemia.

Steinberg MH, Rosenstock W, Coleman MB, Adams JG, Platica O, Cedeno M, Rieder RF, Wilson JT, Milner P, West S. Steinberg MH, et al. Among authors: coleman mb. Blood. 1984 Jun;63(6):1353-60. Blood. 1984. PMID: 6722353 Free article.

7

Beta-thalassemia intermedia with exceptionally high hemoglobin A2: relationship to mutations in the beta-gene promoter.

Coleman MB, Adams JG 3rd, Plonczynski MW, Harrell AH, Walker AM, Fairbanks V, Steinberg MH. Coleman MB, et al. Am J Med Sci. 1992 Aug;304(2):73-8. doi: 10.1097/00000441-199208000-00001. Am J Med Sci. 1992. PMID: 1380206

8

Hb S/beta zero-thalassemia due to the approximately 1.4-kb deletion is associated with a relatively mild phenotype.

Waye JS, Chui DH, Eng B, Cai SP, Coleman MB, Adams JG 3rd, Steinberg MH. Waye JS, et al. Among authors: coleman mb. Am J Hematol. 1991 Oct;38(2):108-12. doi: 10.1002/ajh.2830380207. Am J Hematol. 1991. PMID: 1719807

9

Hemoglobin Terre Haute arginine beta 106. A posthumous correction to the original structure of hemoglobin Indianapolis.

Coleman MB, Steinberg MH, Adams JG 3rd. Coleman MB, et al. J Biol Chem. 1991 Mar 25;266(9):5798-800. J Biol Chem. 1991. PMID: 2005117 Free article.

10

Structural hemoglobin variants that produce the phenotype of thalassemia.

Adams JG 3rd, Coleman MB. Adams JG 3rd, et al. Among authors: coleman mb. Semin Hematol. 1990 Jul;27(3):229-38. Semin Hematol. 1990. PMID: 2197726 Review. No abstract available.

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