Osteogenesis imperfecta (OI) is an inherited disorder of connective tissue involving genes encoding the synthesis of type 1 collagen.[1] Its clinical presentation can vary widely and may include blue scleras (Figure 1), bone fractures, the patient being of short stature, joint and skin laxity, hearing loss and dentition problems..
Osteogenesis imperfecta (OI) is a heterogeneous group of inherited, mostly dominant, disorders chara...
Osteogenesis imperfecta (OI) is the most common genetic bone disorder. The exact incidence of OI is ...
AbstractObjectiveLiterature review of new genes related to osteogenesis imperfecta (OI) and update o...
Osteogenesis imperfecta (OI), an inherited skeletal disorder characterized by low bone mass, bone fr...
Osteogenesis imperfecta or brittle bone disease, a heritable disorder of connective tissue, is the m...
Osteogenesis imperfecta (OI) is a connective tissue disorder that is caused by genetic mutation. OI ...
Osteogenesis imperfecta (OI) is the most frequently occurring congenital disorder with an increased ...
Background: Osteogenesis imperfecta (OI) is a rare, autosomal-inherited, connective tissue disorder ...
Osteogenesis imperfecta (OI) is a hereditary disease of the bones and fascia. It is associated with ...
Osteogenesis imperfecta is a hereditary connective tissue disorder characterized primarily by fractu...
Osteogenesis imperfecta or brittle bone disease, a heritable disorder of connective tissue, is the m...
Bone is a dynamic organ, able to replace old or disrupted tissue through a remodelling process. It c...
Color poster with text, graphs, and images.Osteogenesis imperfecta (OI) has been characterized as bo...
Osteogenesis Imperfecta (OI) is a group of connective tissue disorders with a broad range of phenoty...
O F the group of diseases characterized as generalized 'heritable disorders of connective tissu...
Osteogenesis imperfecta (OI) is a heterogeneous group of inherited, mostly dominant, disorders chara...
Osteogenesis imperfecta (OI) is the most common genetic bone disorder. The exact incidence of OI is ...
AbstractObjectiveLiterature review of new genes related to osteogenesis imperfecta (OI) and update o...
Osteogenesis imperfecta (OI), an inherited skeletal disorder characterized by low bone mass, bone fr...
Osteogenesis imperfecta or brittle bone disease, a heritable disorder of connective tissue, is the m...
Osteogenesis imperfecta (OI) is a connective tissue disorder that is caused by genetic mutation. OI ...
Osteogenesis imperfecta (OI) is the most frequently occurring congenital disorder with an increased ...
Background: Osteogenesis imperfecta (OI) is a rare, autosomal-inherited, connective tissue disorder ...
Osteogenesis imperfecta (OI) is a hereditary disease of the bones and fascia. It is associated with ...
Osteogenesis imperfecta is a hereditary connective tissue disorder characterized primarily by fractu...
Osteogenesis imperfecta or brittle bone disease, a heritable disorder of connective tissue, is the m...
Bone is a dynamic organ, able to replace old or disrupted tissue through a remodelling process. It c...
Color poster with text, graphs, and images.Osteogenesis imperfecta (OI) has been characterized as bo...
Osteogenesis Imperfecta (OI) is a group of connective tissue disorders with a broad range of phenoty...
O F the group of diseases characterized as generalized 'heritable disorders of connective tissu...
Osteogenesis imperfecta (OI) is a heterogeneous group of inherited, mostly dominant, disorders chara...
Osteogenesis imperfecta (OI) is the most common genetic bone disorder. The exact incidence of OI is ...
AbstractObjectiveLiterature review of new genes related to osteogenesis imperfecta (OI) and update o...
DOI
Add to ORKG