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 Disease InfoSearch National Organization for Rare Disorders (NORD) ...
    https://medlineplus.gov/genetics/condition/1q211-microdeletion - Genetics
  2. 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
  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 
    ... the deletion in chromosome 1 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 
    ... duplication on to their children. 1q21.1 duplication 1q21.1 duplication syndrome Genetic Testing Registry: Chromosome 1q21.1 duplication syndrome Chromosome 1q21.1 duplication syndrome Disease InfoSearch National ...
    https://medlineplus.gov/genetics/condition/1q211-microduplication - Genetics