J. Gonzalez‐Redondo

发表

Frameshift codon 5 [Fsc-5 (-CT)] thalassemia; a novel mutation detected in a Greek patient.

D. Loukopoulos, P. Kollia, T. Huisman, 1989, Hemoglobin.

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

A. Kutlar, V. Mckie, F. Kutlar, 1988, Blood.

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

A. Kutlar, V. Mckie, F. Kutlar, 1988 .

Severe Hb S‐β°‐thalassaemia with a T → C substitution in the donor splice site of the first intron of the β‐globin gene

A. Kutlar, V. Mckie, K. McKie, 1989 .

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.

A. Kutlar, Y. Fei, M. Aksoy, 1989, Blood.

Abnormal processing of β-Malay globin RNA

H. Brickner, G. Atweh, J. Gonzalez‐Redondo, 1989 .

Characterization of a New α-Thalassemia-1 Deletion in a Spanish Family

F. Gilsanz, J. Gonzalez‐Redondo, P. Ricard, 1989 .

Characterization of a newly discovered α‐thalassaemia‐1 in two Spanish patients with Hb H disease

J. Díaz-Chico, T. Huisman, J. J. Malcorra-Azpiazu, 1988, British journal of haematology.

Nucleotide Sequence of the Human 01-Globin Gene

T. Huisman, I. Han, J. Gonzalez‐Redondo, 1988 .

Nucleotide sequence of the humanθ1-globin gene

T. Huisman, I. Han, Y. Gu, 1988, Biochemical Genetics.

Molecular characterization of β‐thalassaemia in 174 Greek patients with thalassaemia major

A. Kutlar, C. Kattamis, T. Huisman, 1990, British journal of haematology.

Beta-thalassemia due to a T----A mutation within the ATA box.

Y. Fei, T. Huisman, A. Gurgey, 1988, Biochemical and biophysical research communications.

Molecular characterization of Hb S(C) β‐thalassemia in American blacks

A. Kutlar, T. Huisman, V. Mckie, 1991 .

Hb Monroe or alpha 2 beta 230(B12)Arg----Thr, a variant associated with beta-thalassemia due to A G----C substitution adjacent to the donor splice site of the first intron.

A. Kutlar, T. Huisman, J. B. Wilson, 1989, Hemoglobin.

Hb S(C)‐β+‐thalassaemia: different mutations are associated with different levels of normal Hb A

A. Kutlar, Y. Kilinç, T. Huisman, 1988, British journal of haematology.

The levels of ζ, γ, and δ chains in patients with Hb H disease

A. Kutlar, K. Kleman, A. Gurgey, 1989, Human Genetics.

Hb natal or α2(minus Tyr-Arg)β2: a high oxygen affinity α chain variant with a deleted carboxy-terminus resulting from a TAC → TAA (Tyr→ terminating codon) mutation in codon α140

A. Kutlar, T. Huisman, J. B. Wilson, 1988 .

Abnormal processing of beta-Malay globin RNA.

H. Brickner, G. Atweh, J. Gonzalez‐Redondo, 1989, Biochemical and biophysical research communications.

Molecular characterization of Hb S(C) beta-thalassemia in American blacks.

A. Kutlar, T. Huisman, V. Mckie, 1991, American journal of hematology.

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

A. Kutlar, T. Huisman, K. Kleman, 1989, Human genetics.

Clinical and Molecular Characterization of Thalassemia Intermedia and Thalassemia Major in American Blacks a

T. Huisman, F. Kutlar, A. Kutlar, 1989 .

Hb Icaria–Hb H disease: identification of the Hb Icaria mutation through analysis of amplified DNA

T. Huisman, C. Oner, J. Codrington, 1990, British journal of haematology.