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chromosome abnormality

См. также в других словарях:

  • Chromosome abnormality — The three major single chromosome mutations; deletion (1), duplication (2) and inversion (3) …   Wikipedia

  • Chromosome engineering — is the controlled generation of chromosomal deletions, inversions, or translocations with defined endpoints. [1] By combining chromosomal translocation, chromosomal inversion,and chromosomal deletion, chromosome engineering has been shown to… …   Wikipedia

  • Chromosome — For a non technical introduction to the topic, see Introduction to genetics. Diagram of a replicated and condensed metaphase eukaryotic chromosome. (1) Chromatid – one of the two identical parts of the chromosome after S phase. (2)… …   Wikipedia

  • Chromosome De Philadelphie — Pour les articles homonymes, voir Ph. Le chromosome Philadelphie (ou de Philadelphie) (Ph) ou translocation de Philadelphie est une anomalie chromosomique spécifique qui est associée à la leucémie myéloïde chronique (LMC). Ceci est le résultat… …   Wikipédia en Français

  • Chromosome de philadelphie — Pour les articles homonymes, voir Ph. Le chromosome Philadelphie (ou de Philadelphie) (Ph) ou translocation de Philadelphie est une anomalie chromosomique spécifique qui est associée à la leucémie myéloïde chronique (LMC). Ceci est le résultat… …   Wikipédia en Français

  • Chromosome 22 (human) — Chromosome 22 is one of the 23 pairs of chromosomes in human cells. Humans normally have two copies of Chromosome 22 in each cell. Chromosome 22 is the second smallest human chromosome, spanning about 49 million DNA base pairs and representing… …   Wikipedia

  • Chromosome 15 (human) — Human chromosome 15 Chromosome 15 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 15 spans about 106 million base pairs (the building material of DNA) and represents between 3% and 3 …   Wikipedia

  • Chromosome disorder — An abnormal condition due to an abnormality of the chromosomes. For example, Down syndrome (the genetic abnormality featuring three chromosome 21s, instead of two, also referred to as trisomy 21) is a chromosome disorder …   Medical dictionary

  • Chromosome de Philadelphie — Pour les articles homonymes, voir Ph. Le chromosome Philadelphie (ou de Philadelphie) (Ph) ou translocation de Philadelphie est une anomalie chromosomique spécifique qui est associée à la leucémie myéloïde chronique (LMC). Ceci est le résultat… …   Wikipédia en Français

  • Ring chromosome 20 syndrome — Ring chromosome 20, ring shaped chromosome 20 or r(20) syndrome is a rare human chromosome abnormality where the two arms of chromosome 20 fuse to form a ring chromosome. The syndrome is associated with epileptic seizures, behaviour disorders and …   Wikipedia

  • Syndrome, chromosome 4 short-arm deletion — This syndrome, called the Wolf Hirschhorn syndrome, is a chromosome disorder due to partial deletion of the short (p) arm of chromosome 4. It is, therefore, also called the 4p syndrome. Features of the syndrome include midline defects with a… …   Medical dictionary

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