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Results 1 - 5 of 5 for maxillary
  1. The SPECC1L gene provides instructions for making a protein called cytospin-A. This protein stabilizes components of the cell's structural framework (cytoskeleton) ...
  2. ... RUNX2 gene causes a disorder called metaphyseal dysplasia, maxillary hypoplasia, and brachydactyly (MDMHB). This condition is characterized ... of long bones (metaphyses), an underdeveloped upper jawbone (maxilla), and short fingers (brachydactyly). Other skeletal abnormalities can ...
  3. ... becomes shaped more like the smaller upper jaw (maxilla). The abnormal shape leads to an unusually small ...
  4. ... becomes shaped more like the smaller upper jaw (maxilla). The abnormal shape leads to an unusually small ...
  5. ... M. SHH mutation is associated with solitary median maxillary central incisor: a study of 13 patients and ...