Chromosome 1q21.1 deletion syndrome

1q21.1 microdeletion syndrome is a newly described recurrent deletion syndrome with variable clinical manifestations but without the clinical picture of thrombocytopenia - absent radius (TAR) syndrome.

Also known as: 1q21.1 microdeletion syndrome, 1q21.1 recurrent microdeletion (susceptibility locus for neurodevelopmental disorders), Del(1)(q21), chromosome 1q21.1 deletion syndrome, isolated cases, monosomy 1q21.1, 1q21.1 microdeletion, chromosome 1q21.1 deletion syndrome, 1.35-MB, chromosome 1q21.1 microdeletion syndrome

1 clinical trial for this condition and its sub-types, 1 tagged with Chromosome 1q21.1 deletion syndrome itself.