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Qu'est-ce (qui) est 7q11 23 duplication syndrome - définition
DUPLICATION OF A GENE SEQUENCE WITHIN A GENOME
Duplicate gene; Chromosomal duplication; Chromosomal duplications; Chromosome duplication; Chromosome duplications; Duplication (genetics); Ancient gene duplication; Amplification (molecular biology); Tandem duplications; Tandem duplication; Duplication (chromosomal); Retrogene; Nucleotide duplication
22q11.2 duplication syndrome
HUMAN DISEASE
22q11 duplication syndrome
22q11.2 duplication syndrome is a rare genetic disorder caused by a duplication of a segment at the end of chromosome 22.
7q11.23 duplication syndrome
MEDICAL CONDITION
Draft:7q11.23 Duplication Syndrome; Dup7
7q11.23 duplication syndrome (also called dup7 or Duplication of the Williams-Beuren Syndrome Critical Region) is a rare genetic syndrome caused by micro-duplication of 1.
Gene duplication
Gene duplication (or chromosomal duplication or gene amplification) is a major mechanism through which new genetic material is generated during molecular evolution. It can be defined as any duplication of a region of DNA that contains a gene.
Wikipédia
Gene duplication
Gene duplication (or chromosomal duplication or gene amplification) is a major mechanism through which new genetic material is generated during molecular evolution. It can be defined as any duplication of a region of DNA that contains a gene. Gene duplications can arise as products of several types of errors in DNA replication and repair machinery as well as through fortuitous capture by selfish genetic elements. Common sources of gene duplications include ectopic recombination, retrotransposition event, aneuploidy, polyploidy, and replication slippage.
