Multiple Osteochondromas (MO; previously known as multiple hereditary exostosis) is an autosomal dominant genetic condition that is characterized by the formation of cartilaginous bone tumours (osteochondromas) at multiple sites in the skeleton, secondary bursa formation and impingement of nerves, tendons and vessels, bone curving, and short stature. MO is also known to be associated with arthritis, general pain, scarring and occasional malignant transformation of osteochondroma into secondary peripheral chondrosarcoma. MO patients present additional complains but the relevance of those in relation to the syndromal background needs validation. Mutations in two enzymes that are required during heparan sulphate synthesis (EXT1 or EXT2) are kn...
Bruck syndrome, a disorder caused by recessive mutations in either PLOD2 or FKBP10, is characterized...
Background/Introduction: Skeletal deformities in teleost fish have already been extensively describe...
The type I collagenopathies are a group of heterogeneous connective tissue disorders, that are cause...
Multiple Osteochondromas (MO; previously known as multiple hereditary exostosis) is an autosomal dom...
Multiple Osteochondromas (MO; previously known as multiple hereditary exostosis) is an autosomal dom...
development of osteochondroma, an isolated/sporadic- or a multifocal/hereditary cartilaginous bone t...
Mutations in human Exostosin genes (EXTs) confer a disease called Hereditary Multiple Exostoses (HME...
Osteogenesis imperfecta (OI) is a hereditary brittle bone disorder that is mostly (>90%) caused by d...
Osteogenesis imperfecta (OI) is a hereditary brittle bone disorder that is mostly (>90%) caused by d...
Fragile bone disorders (FBD) are characterized by increased fracture risks due to insufficient or fr...
Introduction: Animal models for OI have proved indispensable for unraveling molecular mechanisms in ...
H6 family homeobox 1 (HMX1) regulates multiple aspects of craniofacial development, and mutations in...
Clinical variability in OI patients carrying an identical causal variant is frequently observed. Thi...
AbstractSystematic identification of skeletal dysplasias in model vertebrates provides insight into ...
Inherited dental malformations constitute a clinically and genetically heterogeneous group of disord...
Bruck syndrome, a disorder caused by recessive mutations in either PLOD2 or FKBP10, is characterized...
Background/Introduction: Skeletal deformities in teleost fish have already been extensively describe...
The type I collagenopathies are a group of heterogeneous connective tissue disorders, that are cause...
Multiple Osteochondromas (MO; previously known as multiple hereditary exostosis) is an autosomal dom...
Multiple Osteochondromas (MO; previously known as multiple hereditary exostosis) is an autosomal dom...
development of osteochondroma, an isolated/sporadic- or a multifocal/hereditary cartilaginous bone t...
Mutations in human Exostosin genes (EXTs) confer a disease called Hereditary Multiple Exostoses (HME...
Osteogenesis imperfecta (OI) is a hereditary brittle bone disorder that is mostly (>90%) caused by d...
Osteogenesis imperfecta (OI) is a hereditary brittle bone disorder that is mostly (>90%) caused by d...
Fragile bone disorders (FBD) are characterized by increased fracture risks due to insufficient or fr...
Introduction: Animal models for OI have proved indispensable for unraveling molecular mechanisms in ...
H6 family homeobox 1 (HMX1) regulates multiple aspects of craniofacial development, and mutations in...
Clinical variability in OI patients carrying an identical causal variant is frequently observed. Thi...
AbstractSystematic identification of skeletal dysplasias in model vertebrates provides insight into ...
Inherited dental malformations constitute a clinically and genetically heterogeneous group of disord...
Bruck syndrome, a disorder caused by recessive mutations in either PLOD2 or FKBP10, is characterized...
Background/Introduction: Skeletal deformities in teleost fish have already been extensively describe...
The type I collagenopathies are a group of heterogeneous connective tissue disorders, that are cause...