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1 als formed one or more ectopic bone growths (exostoses).
2 lation caused dwarfism, chondrodysplasia and exostoses.
3 lar mechanisms underlying the development of exostoses.
4 le therapeutic target in hereditary multiple exostoses.
5 or suppressors linked to hereditary multiple exostoses.
6 alence or characteristics of buccal alveolar exostoses.
7 or suppressors linked to hereditary multiple exostoses.
8 d as marginal bony lippings and 7% as buccal exostoses.
9 ent of Wilm's tumors and hereditary multiple exostoses.
10 y be sufficient to cause hereditary multiple exostoses.
11 re made of the height, width, and breadth of exostoses.
12 hree were idiopathic involving large lingual exostoses.
13 ence and distribution of heparanase in human exostoses.
14 s those in patients with hereditary multiple exostoses.
15 tout-velu, a gene related to the vertebrate Exostoses 1 heparan sulfate co-polymerase, likewise does
16 tion identified novel specific gene targets (exostoses 1) or shRNA constructs capable of altering hum
17 year-old female patient manifesting multiple exostoses and autism accompanied by mental retardation a
18 of individual genes responsible for multiple exostoses and parietal foramina in PSS, the identity of
19 ated patients with either autism or multiple exostoses as well as linkage and association studies is
20 S; MIM 601224) are characterized by multiple exostoses, attributable to haploinsufficiency of EXT2 an
21 The prevalence and features of 3 types of exostoses commonly encountered during periodontal surger
23 rillar collagen are associated with multiple exostoses due to mutation of the EXT1 gene is described.
24 a rare inherited disorder featuring multiple exostoses, enchondromas, joint destruction and bony defo
28 search, abnormalities in hereditary multiple exostoses genes, which encode protein products essential
31 the biological basis of hereditary multiple exostoses (HME), a disease associated with bone overgrow
32 tilaginous outgrowths in Hereditary Multiple Exostoses (HME), a pediatric disorder caused by EXT muta
35 in humans, also known as multiple hereditary exostoses (MHE or HME) and characterized by the formatio
37 romosome 11 and is characterized by multiple exostoses, parietal foramina, intellectual disability (I
39 chondromas obtained from hereditary multiple exostoses patients was much lower than that in hypertrop
41 enesis, lead us to propose that the multiple exostoses syndrome is associated with abnormal diffusion
42 is family are involved in the human multiple exostoses syndrome, which affects bone morphogenesis.
43 erized by benign cartilaginous tumors called exostoses that form next to growing skeletal elements.
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