Add to ORKGCraniometaphyseal dysplasia (CMD) is a rare craniotubular bone dysplasia transmitted in autosomal dominant or recessive form. This disease is characterized by cranial bone hyperosto-sis and deformity of the metaphyses of the long bones. Usin
Mutations in the pyrophosphate (PPi) transporter ANKH cause the autosomal dominant form of craniomet...
We present the clinical and radiographic findings in a patient with the autosomal recessive form of ...
Craniometaphyseal dysplasia (CMD) is a rare skeletal disorder characterized by progressive thickenin...
Craniometaphyseal dysplasia (CMD) is a rare genetically transmitted bone dysplasia characterized by ...
Craniometaphyseal dysplasia (CMD) is a very rare bone disorder of unknown etiology. It is characteri...
Summary: We identified osteoclast defects in craniometaphyseal dysplasia (CMD) using an easy-to-use ...
Craniometaphyseal dysplasia (CMD) is a rare genetic skeletal disorder, whose biological understandin...
We report a 14-month-old male with craniometaphyseal dysplasia (CMD). The patient presented with a h...
AbstractWe report a 14-month-old male with craniometaphyseal dysplasia (CMD). The patient presented ...
Craniometaphyseal dysplasia (CMD) is a rare, sclerosing skeletal disorder caused by mutations in ANK...
Craniotubular dysplasias (CTD) are a heterogeneous group of genetic disorders of skeletal developmen...
Craniometaphyseal dysplasia (CMD; OMIM #123000) is a rare genetic disorder characterized by hyperost...
Cleidocranial dysplasia (CCD) is an autosomal dominant skeletal dysplasia characterized by hypoplast...
Craniometaphyseal dysplasia (CMD) is a rare sclerosing skeletal disorder with progressive hyperostos...
More than 500 rare genetic bone disorders have been described, but for many of them only limited tre...
Mutations in the pyrophosphate (PPi) transporter ANKH cause the autosomal dominant form of craniomet...
We present the clinical and radiographic findings in a patient with the autosomal recessive form of ...
Craniometaphyseal dysplasia (CMD) is a rare skeletal disorder characterized by progressive thickenin...
Craniometaphyseal dysplasia (CMD) is a rare genetically transmitted bone dysplasia characterized by ...
Craniometaphyseal dysplasia (CMD) is a very rare bone disorder of unknown etiology. It is characteri...
Summary: We identified osteoclast defects in craniometaphyseal dysplasia (CMD) using an easy-to-use ...
Craniometaphyseal dysplasia (CMD) is a rare genetic skeletal disorder, whose biological understandin...
We report a 14-month-old male with craniometaphyseal dysplasia (CMD). The patient presented with a h...
AbstractWe report a 14-month-old male with craniometaphyseal dysplasia (CMD). The patient presented ...
Craniometaphyseal dysplasia (CMD) is a rare, sclerosing skeletal disorder caused by mutations in ANK...
Craniotubular dysplasias (CTD) are a heterogeneous group of genetic disorders of skeletal developmen...
Craniometaphyseal dysplasia (CMD; OMIM #123000) is a rare genetic disorder characterized by hyperost...
Cleidocranial dysplasia (CCD) is an autosomal dominant skeletal dysplasia characterized by hypoplast...
Craniometaphyseal dysplasia (CMD) is a rare sclerosing skeletal disorder with progressive hyperostos...
More than 500 rare genetic bone disorders have been described, but for many of them only limited tre...
Mutations in the pyrophosphate (PPi) transporter ANKH cause the autosomal dominant form of craniomet...
We present the clinical and radiographic findings in a patient with the autosomal recessive form of ...
Craniometaphyseal dysplasia (CMD) is a rare skeletal disorder characterized by progressive thickenin...