Results 1 - 5 of 5 for "1q21.1" microdeletion syndrome
  1. ... Mb Genetic Testing Registry: 1q21.1 recurrent microdeletion 1q21.1 microdeletion syndrome Disease InfoSearch National Organization for Rare Disorders (NORD) ...
  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. ...
  3. ... 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 ...
  4. ... 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 ...
  5. ... 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 ...