Add to ORKGcartilage; Hereditary Multiple Exostoses • Heparan sulfate proteoglycans and a number of growth factors they control are expressed and active in the growth plate and surrounding perichondrium • Congenital mutations in HS-synthesizing and modifying enzymes and HSPG expression cause severe skeletal and craniofacial phenotypes • Recent developments in understanding Hereditary Multiple Exostoses (HME) suggest that aberrant growth factor signaling plays a major role in exostosis initiation and growth Funding: NIH RC1AR058382 and R01AR061758
We present a patient diagnosed with a multiple congenital anomaly syndrome characterized by scoliosi...
Multiple osteochondromas (MO) is a hereditary disorder associated with benign cartilaginous tumors, ...
ABSTRACT: Multiple osteochondromas (MO) is an autosomal dominant skeletal disease characterized by t...
Hereditary multiple exostoses (HME) is an inherited genetic condition characterized by the presence ...
Skeletogenesis of the axial and appendicular elements occurs through endochondral ossification, a co...
The different clinical entities of osteochondromas, hereditary multiple exostoses (HME) and non-fami...
Hereditary multiple exostoses (HME), also called hereditary multiple osteochondromas, is a rare gene...
Hereditary multiple exostoses (HME) syndrome is an autosomal dominant inherited human disorder, whic...
Multiple hereditary exostoses (MHE) is an autosomal dominant disorder that affects about 1 in 50,000...
Review on Hereditary multiple exostoses (HME), with data on clinics, and the genes involved
Multiple hereditary exostoses (MHE) is an autosomal dominant disorder that affects about 1 in 50,000...
Background and Objectives: Hereditary multiple exostoses (HME) is a disease characterized by cartila...
Osteochondroma is a cartilage capped benign bone tumour, arising at the external surface of bones pr...
ultiple hereditary exostosis is an autosomal domi-nant inherited disease in which osteochondral grow...
Hereditary multiple exostoses (HME), a dominantly inherited genetic disorder characterized by multi...
We present a patient diagnosed with a multiple congenital anomaly syndrome characterized by scoliosi...
Multiple osteochondromas (MO) is a hereditary disorder associated with benign cartilaginous tumors, ...
ABSTRACT: Multiple osteochondromas (MO) is an autosomal dominant skeletal disease characterized by t...
Hereditary multiple exostoses (HME) is an inherited genetic condition characterized by the presence ...
Skeletogenesis of the axial and appendicular elements occurs through endochondral ossification, a co...
The different clinical entities of osteochondromas, hereditary multiple exostoses (HME) and non-fami...
Hereditary multiple exostoses (HME), also called hereditary multiple osteochondromas, is a rare gene...
Hereditary multiple exostoses (HME) syndrome is an autosomal dominant inherited human disorder, whic...
Multiple hereditary exostoses (MHE) is an autosomal dominant disorder that affects about 1 in 50,000...
Review on Hereditary multiple exostoses (HME), with data on clinics, and the genes involved
Multiple hereditary exostoses (MHE) is an autosomal dominant disorder that affects about 1 in 50,000...
Background and Objectives: Hereditary multiple exostoses (HME) is a disease characterized by cartila...
Osteochondroma is a cartilage capped benign bone tumour, arising at the external surface of bones pr...
ultiple hereditary exostosis is an autosomal domi-nant inherited disease in which osteochondral grow...
Hereditary multiple exostoses (HME), a dominantly inherited genetic disorder characterized by multi...
We present a patient diagnosed with a multiple congenital anomaly syndrome characterized by scoliosi...
Multiple osteochondromas (MO) is a hereditary disorder associated with benign cartilaginous tumors, ...
ABSTRACT: Multiple osteochondromas (MO) is an autosomal dominant skeletal disease characterized by t...
