- X-autosome translocation
- траслокация между Х-хромосомой и аутосомой
Англо-русский словарь промышленной и научной лексики. 2014.
Англо-русский словарь промышленной и научной лексики. 2014.
Chromosomal translocation — of the 4th and 20th chromosome. In genetics, a chromosome translocation is a chromosome abnormality caused by rearrangement of parts between nonhomologous chromosomes. A gene fusion may be created when the translocation joins two otherwise… … Wikipedia
Ohno's law — For the Japanese lexical law, see Ōno s lexical law. Ohno s law was proposed by a Japanese biologist Susumu Ohno, saying that the gene content of the mammalian species has been conserved over species not only in the DNA content but also in the… … Wikipedia
Renal tubular acidosis — Infobox Disease Name = PAGENAME Caption = Significant bilateral nephrocalcinosis (calcification of the kidneys) on a frontal X ray (radiopacities (white) in the right upper and left upper quadrant of the image), as seen in distal renal tubular… … Wikipedia
KLF8 — Kruppel like factor 8, also known as KLF8, is a human gene.cite web | title = Entrez Gene: KLF8 Kruppel like factor 8| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=11279| accessdate = ] PBB Summary… … 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 — [ kromozom ] n. m. • 1889; mot all. 1888, du gr. khrôma « couleur » et sôma « corps », « parce qu [ils] absorbent électivement certaines matières colorantes » (J. Rostand) ♦ Chacun des éléments essentiels du noyau cellulaire, de forme déterminée… … Encyclopédie Universelle
Patau syndrome — Classification and external resources Chromosome 13 ICD 10 Q91.4 Q … Wikipedia
Centromere — Chromosomal components: (1) Chromatid (2) Centromere (3) Short arm (4) Long arm A centromere is a region of DNA typically found near the middle of a chromosome where two identical sister chromatids come closest in contact. It is involved in cell… … Wikipedia
Chromosome 21 (human) — Chromosome 21 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. The trisomy of the 21st chromosome causes Down Syndrome. Chromosome 21 is the smallest human chromosome, 47 million nucleotides… … Wikipedia
X-inactivation — The Barr body is indicated by the arrow, it identifies the inactive X (Xi).] macroH2A1 staining. Arrow points to sex chromatin in DAPI stained cell nucleus, and to the corresponding sex chromatin site in the histone macroH2A1 staining.] X… … Wikipedia
Genetic history of indigenous peoples of the Americas — For a non technical introduction to genetics in general, see Introduction to genetics … Wikipedia