Kutlar A - Search Results

1

One form of inclusion body beta-thalassemia is due to a GAA----TAA mutation at codon 121 of the beta chain.

Fei YJ, Stoming TA, Kutlar A, Huisman TH, Stamatoyannopoulos G. Fei YJ, et al. Among authors: kutlar a. Blood. 1989 Mar;73(4):1075-7. Blood. 1989. PMID: 2563949 Free article. No abstract available.

2

A C----T substitution at nt--101 in a conserved DNA sequence of the promotor region of the beta-globin gene is associated with "silent" beta-thalassemia.

Gonzalez-Redondo JM, Stoming TA, Kutlar A, Kutlar F, Lanclos KD, Howard EF, Fei YJ, Aksoy M, Altay C, Gurgey A, et al. Gonzalez-Redondo JM, et al. Among authors: kutlar f, kutlar a. Blood. 1989 May 1;73(6):1705-11. Blood. 1989. PMID: 2713503 Free article.

3

Inclusion body beta-thalassemia trait in a Swiss family is caused by an abnormal hemoglobin (Geneva) with an altered and extended beta chain carboxy-terminus due to a modification in codon beta 114.

Beris P, Miescher PA, Diaz-Chico JC, Han IS, Kutlar A, Hu H, Wilson JB, Huisman TH. Beris P, et al. Among authors: kutlar a. Blood. 1988 Aug;72(2):801-5. Blood. 1988. PMID: 3401599 Free article.

4

An initiation codon mutation as a cause of a beta-thalassemia.

Jankovic L, Efremov GD, Josifovska O, Juricic D, Stoming TA, Kutlar A, Huisman TH. Jankovic L, et al. Among authors: kutlar a. Hemoglobin. 1990;14(2):169-76. doi: 10.3109/03630269009046958. Hemoglobin. 1990. PMID: 2272840

5

Beta zero-thalassemia in association with a gamma-globin gene quadruplication.

Yang KG, Liu JZ, Kutlar F, Kutlar A, Altay C, Gurgey A, Huisman TH. Yang KG, et al. Among authors: kutlar f, kutlar a. Blood. 1986 Dec;68(6):1394-7. Blood. 1986. PMID: 2430648 Free article.

6

An approximately 300 bp deletion involving part of the 5' beta-globin gene region is observed in members of a Turkish family with beta-thalassemia.

Diaz-Chico JC, Yang KG, Kutlar A, Reese AL, Aksoy M, Huisman TH. Diaz-Chico JC, et al. Among authors: kutlar a. Blood. 1987 Aug;70(2):583-6. Blood. 1987. PMID: 2440502 Free article.

7

Mild and severe beta-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probes.

Diaz-Chico JC, Yang KG, Stoming TA, Efremov DG, Kutlar A, Kutlar F, Aksoy M, Altay C, Gurgey A, Kilinc Y, et al. Diaz-Chico JC, et al. Among authors: kutlar f, kutlar a. Blood. 1988 Jan;71(1):248-51. Blood. 1988. PMID: 2446680 Free article.

8

Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States.

Gonzalez-Redondo JM, Stoming TA, Lanclos KD, Gu YC, Kutlar A, Kutlar F, Nakatsuji T, Deng B, Han IS, McKie VC, et al. Gonzalez-Redondo JM, et al. Among authors: kutlar f, kutlar a. Blood. 1988 Sep;72(3):1007-14. Blood. 1988. PMID: 2458145 Free article.

9

Reverse dot-blot detection of the African-American beta-thalassemia mutations.

Sutcharitchan P, Saiki R, Huisman TH, Kutlar A, McKie V, Erlich H, Embury SH. Sutcharitchan P, et al. Among authors: kutlar a. Blood. 1995 Aug 15;86(4):1580-5. Blood. 1995. PMID: 7632967 Free article.

10

Beta-thalassemia in Turkey.

Oner R, Altay C, Gurgey A, Aksoy M, Kilinç Y, Stoming TA, Reese AL, Kutlar A, Kutlar F, Huisman TH. Oner R, et al. Among authors: kutlar f, kutlar a. Hemoglobin. 1990;14(1):1-13. doi: 10.3109/03630269009002250. Hemoglobin. 1990. PMID: 2200760 Review.

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