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 abnormality — The three major single chromosome mutations; deletion (1), duplication (2) and inversion (3) … Wikipedia
MUTATIONS — Au niveau de toute reproduction biologique, deux tendances contradictoires sont toujours associées. L’une tend à maintenir immuables les caractères héréditaires; l’autre tend, au contraire, à introduire des changements ou variations génétiques,… … Encyclopédie Universelle
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
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
Chromosome 19 (human) — Chromosome 19 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 19 spans more than 63 million base pairs (the building material of DNA) and represents between 2 and 2.5 percent of the… … Wikipedia
Chromosome 1 (human) — Map of Chromosome 1 Chromosome 1 is the designation for the largest human chromosome. Humans have two copies of chromosome 1, as they do with all of the autosomes, which are the non sex chromosomes. Chromosome 1 spans about 247 million nucleotide … 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
Chromosome — A visible carrier of the genetic information. The 3 billion bp (base pairs) in the human genome are organized into 24 distinct, physically separate microscopic units called chromosomes. All genes are arranged linearly along the chromosomes. The… … Medical dictionary
Mutations génétiques — Mutation (génétique) Pour les articles homonymes, voir mutation. Les mécanismes de l évolution biologique Mécanismes non aléatoires … Wikipédia en Français
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
