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Results 1 - 10 of 21 for Growth abnormality
  1. ... A. Fibroblast growth factor receptor and platelet-derived growth factor receptor abnormalities in eosinophilic myeloproliferative disorders. Acta Haematol. 2008;119( ...
  2. ... and development. These effects include intellectual disability, slow growth, distinctive facial features, weak muscle tone (hypotonia), skeletal abnormalities, and heart defects.Several different changes involving chromosome ...
  3. ... on health and development, including intellectual disability, slow growth, characteristic facial features, weak muscle tone (hypotonia), and abnormalities of the fingers and toes. Changes in chromosome ...
  4. ... or structure of chromosome 7 can cause delayed growth and development, intellectual disability, distinctive facial features, skeletal abnormalities, delayed speech, and other medical problems. Changes in ...
  5. ... that the proteins produced from them promote uncontrolled growth of cells. National Human Genome Research Institute: Chromosome Abnormalities PubMed Audenet F, Attalla K, Sfakianos JP. The ...
  6. ... cancers, the specific genetic changes related to cancer growth are unknown. National Human Genome Research Institute: Chromosome Abnormalities PubMed Barbouti A, Stankiewicz P, Nusbaum C, Cuomo ...
  7. ... family. Affected individuals may have distinctive facial features, growth problems, mild to moderate intellectual disability, developmental delay, genital abnormalities in males, or skeletal or heart defects.People ...
  8. ... overactivates WHSC1, which appears to promote the uncontrolled growth and division of cancer cells. National Human Genome Research Institute: Chromosome Abnormalities PubMed Bergemann AD, Cole F, Hirschhorn K. The ...
  9. ... the 13q14 region may cause intellectual disability, slow growth, and characteristic facial features such as prominent eyebrows, a broad nasal bridge, a short nose, and ear abnormalities. A loss of several genes is likely responsible ...
  10. ... SHOX that is important for bone development and growth. The SHOX gene is located in the pseudoautosomal regions of the sex chromosomes. Having only one copy of this gene likely causes short stature and skeletal abnormalities seen in individuals with Turner syndrome. More About ...
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