Between 1978 and 2009, we studied 1,863 Mexican Mestizo patients with clinical data compatible with a hemoglobinopathy. Of these patients, 382 had some hemoglobin (Hb) abnormality (20.5%), 128 had a sickle cell hemoglobinopathy, representing a general frequency of 6.9%, which is similar to the percentage observed in previous studies on Mexican Mestizos. We analyzed the 5? ?-globin haplotype (5?Hp) in 79 unrelated ?S chromosomes (26 ?S/?S, 14 ?S/?Thal, nine ?S/? A and four ?S/?D), and four haplotypes were observed: 72.2% CAR 24.1% Benin, 2.5% Senegal and 1.2% Cameroon; the last two are reported for first time in Mexico. In some Latin American populations such as Brazil, the Bantu haplotype predominates, while in others such as Jamaica, the B...
Abstract Sickle cell hemoglobin is the result of a mutation at the sixth amino acid position of the ...
Abstract Sickle cell hemoglobin is the result of a mutation at the sixth amino acid position of the ...
Objective: The purpose of this study was to determine the β-globin cluster haplotype variability of ...
Between 1978 and 2009, we studied 1,863 Mexican Mestizo patients with clinical data compatible with ...
?-globin haplotypes of 20 -thalassemia (?-thal) and 87 ?(A) Mexican mestizo chromosomes were analyz...
p. 1283-1288ßS-Globin haplotypes were studied in 80 (160 ßS chromosomes) sickle cell disease patient...
?-Globin haplotypes have been used to investigate the origin and spread of ?-globin mutations such a...
To investigate the origin of the ? A and ? S genes in a Mexican population with African roots and a ...
Introduction. Hemoglobin disorders are classified into three main groups: structural variants, thala...
Five restriction site polymorphisms in the β-globin gene cluster (HincII-5'ε, HindIII-G	...
Twenty-five individuals were studied from four unrelated Mexican Mestizo families with Hb D-Los Ange...
The haplotypes of 97 βA independent chromosomes from a Mexican Huichol Native American group were an...
ßS-Globin haplotypes were studied in 80 (160 ßS chromosomes) sickle cell disease patients from Salva...
ßS-Globin haplotypes were studied in 80 (160 ßS chromosomes) sickle cell disease patients from Salva...
Twenty-five individuals were studied from four unrelated Mexican Mestizo families with Hb D-Los Ange...
Abstract Sickle cell hemoglobin is the result of a mutation at the sixth amino acid position of the ...
Abstract Sickle cell hemoglobin is the result of a mutation at the sixth amino acid position of the ...
Objective: The purpose of this study was to determine the β-globin cluster haplotype variability of ...
Between 1978 and 2009, we studied 1,863 Mexican Mestizo patients with clinical data compatible with ...
?-globin haplotypes of 20 -thalassemia (?-thal) and 87 ?(A) Mexican mestizo chromosomes were analyz...
p. 1283-1288ßS-Globin haplotypes were studied in 80 (160 ßS chromosomes) sickle cell disease patient...
?-Globin haplotypes have been used to investigate the origin and spread of ?-globin mutations such a...
To investigate the origin of the ? A and ? S genes in a Mexican population with African roots and a ...
Introduction. Hemoglobin disorders are classified into three main groups: structural variants, thala...
Five restriction site polymorphisms in the β-globin gene cluster (HincII-5'ε, HindIII-G	...
Twenty-five individuals were studied from four unrelated Mexican Mestizo families with Hb D-Los Ange...
The haplotypes of 97 βA independent chromosomes from a Mexican Huichol Native American group were an...
ßS-Globin haplotypes were studied in 80 (160 ßS chromosomes) sickle cell disease patients from Salva...
ßS-Globin haplotypes were studied in 80 (160 ßS chromosomes) sickle cell disease patients from Salva...
Twenty-five individuals were studied from four unrelated Mexican Mestizo families with Hb D-Los Ange...
Abstract Sickle cell hemoglobin is the result of a mutation at the sixth amino acid position of the ...
Abstract Sickle cell hemoglobin is the result of a mutation at the sixth amino acid position of the ...
Objective: The purpose of this study was to determine the β-globin cluster haplotype variability of ...