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The list of organisms by chromosome count describes ploidy or numbers of chromosomes in the cells of various plants, animals, protists, and other living organisms. This number, along with the visual appearance of the chromosome, is known as the karyotype , [ 1 ] [ 2 ] [ 3 ] and can be found by looking at the chromosomes through a microscope .
Download as PDF; Printable version; In other projects Wikidata item; Appearance. move to sidebar hide. Half-lives (example: Gd) 145 ... {isotope colour chart}}
Three chromosomal abnormalities with ISCN nomenclature, with increasing complexity: (A) A tumour karyotype in a male with loss of the Y chromosome, (B) Prader–Willi Syndrome i.e. deletion in the 15q11-q12 region and (C) an arbitrary karyotype that involves a variety of autosomal and allosomal abnormalities. [3]
The following articles are lists of human Y-chromosome DNA haplogroups found in populations around the world. Y-DNA haplogroups by ethnic group; Y-DNA haplogroups in populations of Europe; Y-DNA haplogroups in populations of the Caucasus; Y-DNA haplogroups in populations of the Near East; Y-DNA haplogroups in populations of North Africa
Chromosomes display a banded pattern when treated with some stains. Bands are alternating light and dark stripes that appear along the lengths of chromosomes. Unique banding patterns are used to identify chromosomes and to diagnose chromosomal aberrations, including chromosome breakage, loss, duplication, translocation or inverted segments.
The human genome has been sequenced, as well as the chimpanzee genome. Humans have 23 pairs of chromosomes, while chimpanzees, gorillas and orangutans have 24. Human chromosome 2 is a fusion of two chromosomes 2a and 2b that remained separate in the other primates. [9]
This template is used in the articles for superheavy elements to produce the sortable lists of isotopes. It was created to simplify formatting and standardize references. For each isotope, a row {{ isotopes summary/isotope }} is to be added.
In human genetics, a human Y-chromosome DNA haplogroup is a haplogroup defined by specific mutations in the non-recombining portions of DNA on the male-specific Y chromosome (Y-DNA). Individuals within a haplogroup share similar numbers of short tandem repeats (STRs) and single-nucleotide polymorphisms (SNPs). [ 2 ]