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Results 1 - 9 of 9 for Chromosome 1p36 deletion syndrome
  1. 1p36 deletion syndrome 
    ... health problems that are characteristic of this disorder. Chromosome 1p36 deletion syndrome Distal monosomy 1p36 Monosomy 1p36 syndrome Genetic Testing ...
    https://medlineplus.gov/genetics/condition/1p36-deletion-syndrome - Genetics
  2. Chromosome 1 
    ... in the structure or number of copies of chromosome 1. 1p36 deletion syndrome is caused by a deletion of genetic material ... includes the tip of the p arm of chromosome 1. The size of the deletion varies ... of 1p36 deletion syndrome are likely caused by the loss of multiple ...
    https://medlineplus.gov/genetics/chromosome/1 - Genetics
  3. Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart 
    ... in the development of multiple organs affected in chromosome 1p36 deletions. PLoS One. 2013;8(2):e57460. doi: 10. ...
    https://medlineplus.gov/...thout-anomalies-of-the-brain-eye-or-heart - Genetics
  4. RERE gene 
    ... in the development of multiple organs affected in chromosome 1p36 deletions. PLoS One. 2013;8(2):e57460. doi: 10. ...
    https://medlineplus.gov/genetics/gene/rere - Genetics
  5. Developmental Disabilities (National Library of Medicine)  
    Developmental disabilities are severe, long-term problems. They may be physical, such as blindness. They may affect mental ability, such as learning disabilities. ...
    https://medlineplus.gov/developmentaldisabilities.html - Health Topics
  6. KIF1B gene 
    ... get rid of cells it does not need. Deletion of a region of chromosome 1 containing the KIF1B gene, designated 1p36, has been identified in some people with neuroblastoma, ...
    https://medlineplus.gov/genetics/gene/kif1b - Genetics
  7. Neuroblastoma 
    ... as a haploinsufficient tumor suppressor gene mapped to chromosome 1p36.2 by inducing apoptotic cell death. J Biol ...
    https://medlineplus.gov/genetics/condition/neuroblastoma - Genetics
  8. Polymicrogyria 
    ... and multiple birth defects. These include 22q11.2 deletion syndrome, Adams-Oliver syndrome, Aicardi syndrome, Galloway-Mowat syndrome, ... Leventer RJ, Pilz DT, Dobyns WB. Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical ...
    https://medlineplus.gov/genetics/condition/polymicrogyria - Genetics
  9. Patient support and advocacy groups 
    ... Research and Resource Group 15q13.3 Research Project 1p36 Deletion Support & Awareness 22q Family Foundation 3q29 Deletion and ... Chromosome 18 Registry & Research Society Chromosome 22 Central Chromosome 9 ... Colon Cancer Alliance Congenital Hyperinsulinism International Congenital ...
    https://medlineplus.gov/about/general/genetics/supportadvocacygroups -