routine deletion

routine deletion
Компьютерная техника: регулярное удаление (например, временных файлов)

Универсальный англо-русский словарь. . 2011.

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Смотреть что такое "routine deletion" в других словарях:

  • 22q11.2 deletion syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 3631 ICD10 = ICD10|D|82|1|d|80 ICD9 = ICD9|279.11, ICD9|758.32 ICDO = OMIM = 188400 MedlinePlus = eMedicineSubj = med eMedicineTopic = 567 eMedicine mult = eMedicine2|ped|589… …   Wikipedia

  • 1p36 deletion syndrome — Classification and external resources A toddler showing facial symptoms of the syndrome. OMIM 607872 DiseasesDB …   Wikipedia

  • Chromosome 1, 1p36 deletion syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 34535 ICD10 = ICD9 = ICDO = OMIM = 607872 MedlinePlus = eMedicineSubj = eMedicineTopic = eMedicine mult = MeshID = Chromosome 1, 1p36 deletion syndrome is a medical condition caused by a rare …   Wikipedia

  • Distal 18q- — Classification and external resources OMIM 601808 Distal 18q is a genetic condition caused by a deletion of genetic material within one of the two copies of chromosome 18. The deletion involves the distal section of 18q and typically extends to… …   Wikipedia

  • List of programs and machines in the Matrix series — Below is a list composing of all the artificial characters from The Matrix series of science fiction films, comic books and video games.FilmsThe following characters appear primarily in the Matrix films, but many are also present in the comic… …   Wikipedia

  • Hypertrophic cardiomyopathy — Classification and external resources ICD 10 I42.1–I42.2 ICD 9 …   Wikipedia

  • DiGeorge syndrome — 22q11.2 deletion syndrome Classification and external resources Brain computer tomography cuts of t …   Wikipedia

  • Wikipedia:Japan-related topics notice board/New Japan-related articles — Please feel free to list newly created Japan related articles here. Any new articles that have an interesting or unusual fact in them should be suggested for the Did you know? box on the Main Wikipedia page. DYN has a 72 hr. time limit from the… …   Wikipedia

  • 18p- — Classification and external resources OMIM 146390 18p is a genetic condition caused by a deletion of all or part of the short arm (the p arm) of chromosome 18. It occurs in about 1 of every 40,000 births. Contents …   Wikipedia

  • Myelodysplastic syndrome — Classification and external resources ICD 10 D46 ICD 9 238.7 …   Wikipedia

  • heredity — /heuh red i tee/, n., pl. heredities. Biol. 1. the transmission of genetic characters from parents to offspring: it is dependent upon the segregation and recombination of genes during meiosis and fertilization and results in the genesis of a new… …   Universalium


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