Gonzalez Redondo JM - Search Results

1

Hb G-Taipei or beta 22(B4)Glu----Gly in a Chinese family living in The Netherlands.

Landman H, Wilson JB, Kutlar A, Gonzalez Redondo JM, Huisman TH. Landman H, et al. Among authors: gonzalez redondo jm. Hemoglobin. 1987;11(2):169-71. doi: 10.3109/03630268709005793. Hemoglobin. 1987. PMID: 3623978 No abstract available.

2

Hb F-Clarke or alpha 2G gamma 2(65)(E9)Lys----Asn.

Kutlar A, Kutlar F, Wilson JB, Webber BB, Gonzalez Redondo JM, Huisman TH. Kutlar A, et al. Among authors: gonzalez redondo jm. Hemoglobin. 1987;11(2):185-8. doi: 10.3109/03630268709005797. Hemoglobin. 1987. PMID: 2442123 No abstract available.

3

Hb E-Saskatoon or alpha 2 beta 2(22)(B4)Glu----Lys in a Spanish family.

Gonzalez Redondo JM, Sicilia A, Murga MJ, Kutlar A, Wilson JB, Huisman TH. Gonzalez Redondo JM, et al. Hemoglobin. 1987;11(1):35-8. doi: 10.3109/03630268709036579. Hemoglobin. 1987. PMID: 3108201 No abstract available.

4

Hb J-Pontoise or alpha 2(63)(E12)Ala----Asp beta 2 in four members of a Spanish family.

Gonzalez Redondo JM, Wilson JB, Kutlar A, Huisman TH, Sicilia A, Romero C, Fernandes Fuertes I. Gonzalez Redondo JM, et al. Hemoglobin. 1987;11(1):47-50. doi: 10.3109/03630268709036582. Hemoglobin. 1987. PMID: 3583765 No abstract available.

5

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.

Gonzalez-Redondo JM, Stoming TA, Kutlar F, Kutlar A, Hu H, Wilson JB, Huisman TH. Gonzalez-Redondo JM, et al. Hemoglobin. 1989;13(1):67-74. doi: 10.3109/03630268908998053. Hemoglobin. 1989. PMID: 2539344 No abstract available.

6

Molecular characterization of beta-globin gene mutations in Malay patients with Hb E-beta-thalassaemia and thalassaemia major.

Yang KG, Kutlar F, George E, Wilson JB, Kutlar A, Stoming TA, Gonzalez-Redondo JM, Huisman TH. Yang KG, et al. Among authors: gonzalez redondo jm. Br J Haematol. 1989 May;72(1):73-80. doi: 10.1111/j.1365-2141.1989.tb07655.x. Br J Haematol. 1989. PMID: 2736244

7

Characterization of three types of beta zero-thalassemia resulting from a partial deletion of the beta-globin gene.

Gonzalez-Redondo JM, Kattamis C, Huisman TH. Gonzalez-Redondo JM, et al. Hemoglobin. 1989;13(4):377-92. doi: 10.3109/03630268909003400. Hemoglobin. 1989. PMID: 2753736

8

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. Kutlar F, et al. Among authors: gonzalez redondo jm. Hum Genet. 1989 May;82(2):179-86. doi: 10.1007/BF00284054. Hum Genet. 1989. PMID: 2566576

9

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

Kollia P, Gonzalez-Redondo JM, Stoming TA, Loukopoulos D, Politis C, Huisman TH. Kollia P, et al. Among authors: gonzalez redondo jm. Hemoglobin. 1989;13(6):597-604. doi: 10.3109/03630268908993110. Hemoglobin. 1989. PMID: 2606727

10

Hb natal or alpha 2(minus Tyr-Arg) beta 2: a high oxygen affinity alpha chain variant with a deleted carboxy-terminus resulting from a TAC----TAA (Tyr----terminating codon) mutation in codon alpha 140.

Jogessar VB, Westermeyer K, Webber BB, Wilson JB, Hu H, Gonzalez-Redondo JM, Kutlar A, Huisman TH. Jogessar VB, et al. Among authors: gonzalez redondo jm. Biochim Biophys Acta. 1988 Nov 10;951(1):36-41. doi: 10.1016/0167-4781(88)90022-x. Biochim Biophys Acta. 1988. PMID: 3191134

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