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Results 1 - 5 of 5 for "1q21.1" microdeletion syndrome
  1. 1q21.1 microdeletion 
    ... Genetic Testing Registry: Chromosome 1q21.1 deletion syndrome 1q21.1 microdeletion syndrome National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...
    https://medlineplus.gov/genetics/condition/1q211-microdeletion - Genetics
  2. Developmental Disabilities (National Library of Medicine)  
    What are developmental disabilities? Developmental disabilities are conditions that are usually present at birth. They can affect a child's growth and ...
    https://medlineplus.gov/developmentaldisabilities.html - Health Topics
  3. Thrombocytopenia-absent radius syndrome 
    ... kb deletion occurs. The chromosomal change related to 1q21.1 microdeletion is often called the recurrent distal 1.35-Mb deletion. RBM8A chromosome 1 TAR syndrome is inherited in an autosomal recessive pattern, which ...
    https://medlineplus.gov/.../thrombocytopenia-absent-radius-syndrome - Genetics
  4. Chromosome 1 
    ... in chromosome 1 that is associated with TAR syndrome as the 200-kb deletion to distinguish it from another chromosomal abnormality called a 1q21.1 microdeletion (described above). People with a 1q21.1 microdeletion ...
    https://medlineplus.gov/genetics/chromosome/1 - Genetics
  5. 1q21.1 microduplication 
    ... syndrome Genetic Testing Registry: Chromosome 1q21.1 duplication syndrome 1q21.1 microduplication syndrome National Organization for Rare Disorders (NORD) ...
    https://medlineplus.gov/genetics/condition/1q211-microduplication - Genetics