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  2. Chromosome abnormality - Wikipedia

    en.wikipedia.org/wiki/Chromosome_abnormality

    When the chromosome's structure is altered, this can take several forms: [16] Deletions: A portion of the chromosome is missing or has been deleted. Known disorders in humans include Wolf–Hirschhorn syndrome, which is caused by partial deletion of the short arm of chromosome 4; and Jacobsen syndrome, also called the terminal 11q deletion ...

  3. Wolf–Hirschhorn syndrome - Wikipedia

    en.wikipedia.org/wiki/Wolf–Hirschhorn_syndrome

    A more uncommon cause for WHS is the formation of a ring chromosome. A ring chromosome can form when a chromosome breaks apart and forms a circular structure to fuse together. That process may initiate gene loss towards the ends of the chromosome. [9] Severity of symptoms and expressed phenotype differ based on the amount of genetic material ...

  4. Chromosomal deletion syndrome - Wikipedia

    en.wikipedia.org/wiki/Chromosomal_deletion_syndrome

    The chromosomal basis of Wolf-Hirschhorn syndrome (WHS) consists of a deletion of the most terminal portion of the short arm of chromosome 4. The deleted segment of reported individuals represent about one half of the p arm, occurring distal to the bands 4p15.1-p15.2. The proximal boundary of the WHSCR was defined by a 1.9 megabase terminal ...

  5. List of genetic disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_genetic_disorders

    The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child. There are over 6,000 known genetic disorders in humans.

  6. 9q34.3 deletion syndrome - Wikipedia

    en.wikipedia.org/wiki/9q34.3_deletion_syndrome

    Medical genetics Symptoms: Arched eyebrows, small head circumference, midface hypoplasia, prominent jaw and a pouting lower lip. [1] Causes: Genetics. Diagnostic method: Fluorescence in situ hybridization, multiplex ligation-dependent probe amplification, array comparative genomic hybridization, and EHMT1 sequencing. [2] Differential diagnosis

  7. Yeast artificial chromosome - Wikipedia

    en.wikipedia.org/wiki/Yeast_artificial_chromosome

    Yeast artificial chromosomes (YACs) are genetically engineered chromosomes derived from the DNA of the yeast, Saccharomyces cerevisiae, which is then ligated into a bacterial plasmid. By inserting large fragments of DNA, from 100–1000 kb, the inserted sequences can be cloned and physically mapped using a process called chromosome walking .

  8. Saccharomyces cerevisiae - Wikipedia

    en.wikipedia.org/wiki/Saccharomyces_cerevisiae

    The yeast genome is highly accessible to manipulation, hence it is an excellent model for genome engineering. The international Synthetic Yeast Genome Project (Sc2.0 or Saccharomyces cerevisiae version 2.0) aims to build an entirely designer, customizable, synthetic S. cerevisiae genome from

  9. Chromosome 4 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_4

    Chromosome 4 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. People normally have two copies of this chromosome. Chromosome 4 spans more than 190 million base pairs (the building material of DNA ) and represents between 6 and 6.5 percent of the total DNA in cells .