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Related to deletion: deletion syndrome, Deletion mutation
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1p36 Deletion Syndrome is a chromosome disorder that can be characterized by moderate to severe intellectual disability, delayed growth, low muscle tone, limited speech ability and distinct facial features.
2 deletion syndrome was previously known by a number of clinical names such as DiGeorge syndrome (DGS), velocardiofacial syndrome (VCFS), conotruncal anomaly face syndrome (CTAF), Opitz G/BBB syndrome and Cayler cardiofacial syndrome before the underlying chromosomal cause was identified.
Our findings suggest that deletion from the S&P 500 constrains access and/or the cost of financing, and firms respond by increasing their cash holdings.
22q11 deletion syndrome is considered one of the most common chromosomal deletions associated with birth defects and leads to a wide range of health problems, from heart defects to behavioral disorders.
This genetic deletion is found on chromosome 22 where the APOBEC genes, APOBEC3A and APOBEC3B, sit next to each other.
13] did not find the same picture in their cohort of black patients, reporting a deletion detection rate similar to that in the literature (25/40; 62%).
An RCN value below the lower limit of the CI for a locus was considered to indicate deletion of that particular locus.
Each FISH assay included normal lung tissue sections as a negative control, and sections of non-small cell lung carcinoma previously identified as carrying p16 deletion as a positive control.
Homozygosity for the Mediterranean a-thalassemic deletion (hemoglobin Barts hydrops fetalis).
Four conserved deletions were shown among all HP-PRRSVs, including an adenosine deletion at position 122 in the 5'-untranslated region, a guanosine deletion at position 15,278 in the 3'untranslated region, and 2 discontinuous deletions in the NSP-2, including a single amino acid deletion at position 482 ([L.