Search Results - "Ahmed, Nazish Rafique"

Hemoglobin A2 (HbA2) has a measure of unreliability in diagnosing β-thalassemia trait (β-TT) by Al-Amodi, Amani M., Ghanem, Neda Z., Aldakeel, Sumayh A., Ibrahim Al Asoom, Lubna, Rafique Ahmed, Nazish, Almandil, Noor B., Naserullah, Zaki A., Al-Jarrash, Sana, Shakil Akhtar, Mohammed, AbdulAzeez, Sayed, Al-Ali, Amein K., Borgio, J. Francis

“…Introduction: Detection of β-thalassemia trait or carriers (β-TT) depends significantly on an increase in Hemoglobin A 2 (HbA 2 ) levels, which is found at low…”
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Identification of seven novel variants in the β-globin gene in transfusion-dependent and normal patients by Aldakeel, Sumayh A, Ghanem, Neda Z, Al-Amodi, Amani M, Osman, Ahoud Khalid, Al Asoom, Lubna Ibrahim, Ahmed, Nazish Rafique, Almandil, Noor B, Akhtar, Mohammed Shakil, Azeez, Sayed Abdul, Borgio, J Francis

“…Abnormality in results in an inherited recessive blood disorder, which can be caused by variants at the transcriptional or translational level affecting the…”
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Hemoglobin A 2 (HbA 2 ) has a measure of unreliability in diagnosing β-thalassemia trait (β-TT) by Al-Amodi, Amani M, Ghanem, Neda Z, Aldakeel, Sumayh A, Ibrahim Al Asoom, Lubna, Rafique Ahmed, Nazish, Almandil, Noor B, Naserullah, Zaki A, Al-Jarrash, Sana, Shakil Akhtar, Mohammed, AbdulAzeez, Sayed, Al-Ali, Amein K, Borgio, J Francis

“…Detection of β-thalassemia trait or carriers (β-TT) depends significantly on an increase in Hemoglobin A (HbA ) levels, which is found at low levels (<3%) in…”
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