- chain defect
- Полимеры: дефект цепи
Универсальный англо-русский словарь. Академик.ру. 2011.
chain defect
Смотреть что такое "chain defect" в других словарях:
defect — de·fect / dē ˌfekt, di fekt/ n: something or a lack of something that results in incompleteness, inadequacy, or imperfection: as a: a flaw in something (as a product) esp. that creates an unreasonable risk of harm in its normal use see also… … Law dictionary
Chain Reaction (label) — Chain Reaction Filiale de Basic Channel Fondé en 1995 Fondateur Basic Channel Genre(s) Dub Techno … Wikipédia en Français
chain of being — The Great Chain of Being is the title of a book by the American philosopher and historian of ideas A. O. Lovejoy (1873–1962), in which he explored the Neoplatonic and medieval notion of a hierarchy of actual existent things, ordered from the… … Philosophy dictionary
Congenital heart defect — Classification and external resources The normal structure of the heart (left) in comparison to two common locations for a ventricular septal defect (right), the most common form of congenital heart defect.[1] … Wikipedia
Heavy chain disease — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 442 DiseasesDB mult = DiseasesDB2|32226 | ICD10 = ICD10|C|88|1|c|81 ICD10|C|88|2|c|81 ICD9 = ICD9|273.2 ICDO = OMIM = MedlinePlus = eMedicineSubj = med eMedicineTopic = 958 eMedicine mult =… … Wikipedia
Interstitial defect — Interstitials are a variety of crystallographic defects, i.e. atoms which occupy a site in the crystal structure at which there is usually not an atom, or two or more atoms sharing one or more lattice sites such that the number of atoms is larger … Wikipedia
long-chain acyl-CoA dehydrogenase (LCAD) deficiency — a defect in mitochondrial beta oxidation due to a mutation in the gene (locus: 2q34 q35) encoding the acyl CoA dehydrogenase that acts on long chain length fatty acids. It is clinically similar to MCAD deficiency, but urinary excretion is of long … Medical dictionary
medium-chain acyl-CoA dehydrogenase (MCAD) deficiency — a defect in mitochondrial beta oxidation due to a mutation in the gene (locus: 1p31) encoding acyl CoA dehydrogenase that acts on medium chain length fatty acids. It is characterized by recurring episodes of hypoglycemia, vomiting, and lethargy,… … Medical dictionary
genetic defect — noun a disease or disorder that is inherited genetically • Syn: ↑genetic disease, ↑genetic disorder, ↑genetic abnormality, ↑congenital disease, ↑inherited disease, ↑inherited disorder, ↑hereditary disease, ↑ … Useful english dictionary
Mitochondrial respiratory chain disorders — ▪ Table Mitochondrial respiratory chain disorders affected system and organs signs and symptoms nervous low muscle tone, seizures, stroke like episodes, disturbance of balance, peripheral nerve damage, hearing loss eyes cataracts, retinal… … Universalium
short-chain acyl-CoA dehydrogenase (SCAD) deficiency — a defect in mitochondrial beta oxidation due to a mutation in the gene (locus: 12q22 qter) encoding the acyl CoA dehydrogenase that acts on short chain length fatty acids. Clinical presentation is variable, but myopathy and abnormalities of… … Medical dictionary
