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Results 1 - 6 of 6 for Chromosome "1q21.1" deletion syndrome
  1. 1q21.1 microdeletion 
    ... 1q21.1 contiguous gene deletion 1q21.1 deletion Chromosome 1q21.1 deletion syndrome Chromosome 1q21.1 deletion syndrome, 1.35-Mb Genetic Testing Registry: Chromosome 1q21. ...
    https://medlineplus.gov/genetics/condition/1q211-microdeletion - Genetics
  2. Thrombocytopenia-absent radius syndrome 
    ... not show signs and symptoms of the condition. Chromosome 1q21.1 deletion syndrome, 200-KB Radial aplasia-amegakaryocytic thrombocytopenia Radial aplasia- ...
    https://medlineplus.gov/.../thrombocytopenia-absent-radius-syndrome - Genetics
  3. Chromosome 1 
    ... can occur. More About This Health Condition A deletion in the 1q21.1 region of chromosome 1 is involved in most cases of thrombocytopenia-absent radius (TAR) syndrome. TAR syndrome is characterized by the absence of ...
    https://medlineplus.gov/genetics/chromosome/1 - Genetics
  4. RBM8A gene 
    ... 8A in cells. The deletions involved in TAR syndrome eliminate at least 200,000 DNA building blocks (200 kilobases, or 200 kb) from the long (q) arm of chromosome 1 in a region called 1q21.1. The deletion eliminates one copy of the RBM8A gene in ...
    https://medlineplus.gov/genetics/gene/rbm8a - Genetics
  5. 1q21.1 microduplication 
    ... duplication 1q21.1 duplication syndrome Genetic Testing Registry: Chromosome 1q21.1 duplication syndrome 1q21.1 microduplication syndrome National Organization for Rare ...
    https://medlineplus.gov/genetics/condition/1q211-microduplication - Genetics
  6. 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