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