The study of G-T polymorphism in COLIA1 gene and osteoporosis in - thalassemia patients
Mona Fayez Abd El Gawad;
Abstract
Β thalassemia is among the most intensively studied monogenic disorder in man. The β thalassaemias are considered autosomal recessive disorders since the inheritance of two abnormal β globin genes is required to produce a clinically detectable phe
Other data
| Title | The study of G-T polymorphism in COLIA1 gene and osteoporosis in - thalassemia patients | Authors | Mona Fayez Abd El Gawad | Keywords | The study of G-T polymorphism in COLIA1 gene and osteoporosis in - thalassemia patients | Issue Date | 2007 | Description | Β thalassemia is among the most intensively studied monogenic disorder in man. The β thalassaemias are considered autosomal recessive disorders since the inheritance of two abnormal β globin genes is required to produce a clinically detectable phe |
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