Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Prachi Atmapoojya"'
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 11, Iss 1 (2019)
Abstract Sickle Cell Disease (SCD) is a group of inherited single-gene autosomal recessive disorders caused by the ‘sickle’ gene, which affects haemoglobin structure. Sickle cell anemia is the most common hemoglobinopathy worldwide. The burde
Externí odkaz:
https://doaj.org/article/90ed2690fdba426885a0b5beeb4fc211
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases
Mediterranean Journal of Hematology and Infectious Diseases, Vol 11, Iss 1 (2019)
Mediterranean Journal of Hematology and Infectious Diseases, Vol 11, Iss 1 (2019)
Sickle Cell Disease (SCD) is a group of inherited single-gene autosomal recessive disorders caused by the ‘sickle’ gene, which affects haemoglobin structure. Sickle cell anemia is the most common hemoglobinopathy worldwide. The burden of sickle c
Publikováno v:
International Journal Of Medical Science And Clinical Invention.
Autor:
Shyam Srinivasan, Devanand gulab Chaudhari, Prachi Atmapoojya, Sabri Ahsan, Yugesh Kumar Agarwal
Publikováno v:
International Journal of Orthopaedics Sciences. 3:109-110
Fibrodysplasia ossificans progressiva (FOP), a rare and disabling genetic condition characterized by congenital malformations of the great toes and progressive heterotopic endochondral ossification (HEO) which is the most catastrophic of HEO disorder