Background – Sickle cell anemia is one of the most common heritable hematologic diseases affecting humans. Detection of the single base pair mutations at codon 6 of the beta-globin gene is important for the prenatal diagnosis of sickle cell anemia and sickle cell disease. We applied the polymerase chain reaction technology to detect sickle cell patients and heterozygous carriers in a group of patients suspected of sickle cell disease. Methods – The sample was composed of 45 normal individuals and 45 unrelated sickle cel
Diagnosis of single gene disorders in isolated single cells can be accomplished after DNA amplificat...
Background: Beta-thalassemia is a common autosomal recessive hereditary disease in the Meditertanean...
WOS: 000303669700003PubMed ID: 22524255Hemoglobinopathies, especially beta-thalassemia (beta-thal), ...
Sickle cell disease (SCD) is an inherited red cell disorder, characterized by the tendency of haemog...
We can detect the b-globin gene sickle cell mutation by using an assay based on the ligase chain rea...
BackgroundThe diagnosis of sickle cell disease (SCD) is made by hemoglobin assays such as high-perfo...
Background: Sickle cell anaemia (SCA) is a hereditary blood disorder caused by a single mutation in ...
Sickle Cell Disease (SCD) is a monogenic hereditary blood disorder caused by a single point mutation...
OBJECTIVE: To evaluate the usefulness of DNA methods to provide a means to precisely genotypically m...
peer reviewedOBJECTIVES: Hemoglobin (Hb) disorders consist of thalassemia and Hb structural variants...
Sickle cell anemia is a recessive genetic disease caused by the presence in the red blood cell, of a...
1To whom correspondence should be addressed Although prenatal diagnosis has reduced the number of β-...
The rapid emergence of molecular diagnostic platforms has revolutionized the diagnostic approaches i...
Research question Mutations of the beta-globin gene (HBB) cause beta-thalassaemia and sickle cell an...
In vitro DNA amplification by means of the polymerase chain reaction is currently revolutionizing hu...
Diagnosis of single gene disorders in isolated single cells can be accomplished after DNA amplificat...
Background: Beta-thalassemia is a common autosomal recessive hereditary disease in the Meditertanean...
WOS: 000303669700003PubMed ID: 22524255Hemoglobinopathies, especially beta-thalassemia (beta-thal), ...
Sickle cell disease (SCD) is an inherited red cell disorder, characterized by the tendency of haemog...
We can detect the b-globin gene sickle cell mutation by using an assay based on the ligase chain rea...
BackgroundThe diagnosis of sickle cell disease (SCD) is made by hemoglobin assays such as high-perfo...
Background: Sickle cell anaemia (SCA) is a hereditary blood disorder caused by a single mutation in ...
Sickle Cell Disease (SCD) is a monogenic hereditary blood disorder caused by a single point mutation...
OBJECTIVE: To evaluate the usefulness of DNA methods to provide a means to precisely genotypically m...
peer reviewedOBJECTIVES: Hemoglobin (Hb) disorders consist of thalassemia and Hb structural variants...
Sickle cell anemia is a recessive genetic disease caused by the presence in the red blood cell, of a...
1To whom correspondence should be addressed Although prenatal diagnosis has reduced the number of β-...
The rapid emergence of molecular diagnostic platforms has revolutionized the diagnostic approaches i...
Research question Mutations of the beta-globin gene (HBB) cause beta-thalassaemia and sickle cell an...
In vitro DNA amplification by means of the polymerase chain reaction is currently revolutionizing hu...
Diagnosis of single gene disorders in isolated single cells can be accomplished after DNA amplificat...
Background: Beta-thalassemia is a common autosomal recessive hereditary disease in the Meditertanean...
WOS: 000303669700003PubMed ID: 22524255Hemoglobinopathies, especially beta-thalassemia (beta-thal), ...