delete

(redirected from Deletions)
Also found in: Dictionary, Thesaurus, Medical, Encyclopedia.
Related to Deletions: duplications
References in periodicals archive ?
EPA proposed the partial deletion of the KMI parcel in June 2017 and held a 30-day public comment period.
Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: Clues to the mechanisms of formation.
Xp21 contiguous gene deletion is a microdeletion syndrome with intellectual disability,congenital adrenal hypoplasia,glyserol kinase deficiency and dystrophinopathy.
1,2 Multiple types of deletions or mutations have been found to influence the clinically observed heterogeneous phenotypes of a-thalassemia cases.
23 If deletions are already present in germinal layer of testis, spermatogenesis would produce very low number of normal sperm and highest ratio of mutations similar to OAT syndrome.
Caption: Common loss Researchers used DNA deletions to trace relationships among human groups by region.
1p36 Deletion Syndrome is not yet on the pre-approved list for government support the way other chromosome disorders, such as Down Syndrome, is.
Here, we report a first case of large deletion with BMD phenotype of an 11-year-old Gujarati boy.
Our primary objective is to test the change in cash holdings after S&P 500 index additions and deletions.
Previous studies in this country have identified deletions in 50% (30/60) of affected boys, using the Southern blotting technique, [11] 42% (46/110) of affected boys using Southern blotting together with mPCR, [12] and 57% (39/68) of affected boys using the Chamberlain and Beggs mPCR approach.
To date, NF1 constitutional deletions have been identified with multiple techniques, such as microsatellite analysis with intragenic markers (21-23), interphase fluorescence in situ hybridization (FISH) analysis via the use of probes within and flanking the NF1 gene (11,22,24,25), multiplex ligation-dependent probe amplification (MLPA) with commerciallyavailable kits (23, 26), and arraycomparative genomic hybridization (27).
Association of p16 homozygous deletions with clinicopathologic characteristics and EGFR/KRAS/p53 mutations in lung adenocarcinoma.