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Results 1 - 3 of 3 for "1q21.1" microdeletion syndrome
  1. ... Genetic Testing Registry: Chromosome 1q21.1 deletion syndrome 1q21.1 microdeletion syndrome National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...
  2. ... 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 ...
  3. ... syndrome Genetic Testing Registry: Chromosome 1q21.1 duplication syndrome 1q21.1 microduplication syndrome National Organization for Rare Disorders (NORD) ...