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Results 1 - 10 of 13 for Chromosome inversion disorder
  1. Recombinant 8 syndrome 
    ... in each cell is sufficient to cause the disorder.Most people with recombinant 8 syndrome have one parent with a change in chromosome 8 called an inversion. An inversion involves the breakage of a chromosome ...
    https://medlineplus.gov/genetics/condition/recombinant-8-syndrome - Genetics
  2. Williams syndrome 
    ... is unaffected, has a chromosomal change called an inversion in the region of ... to cause the disorder. In a small percentage of cases, people with ...
    https://medlineplus.gov/genetics/condition/williams-syndrome - Genetics
  3. X chromosome 
    ... syndrome (MLS): a male with a mosaic paracentric inversion of Xp. Cytogenet Genome Res. 2002;99(1-4):297-302. doi: 10.1159/000071607. Citation on PubMed Lyon MF. X-chromosome inactivation and human genetic disease. Acta Paediatr Suppl. 2002;91(439):107-12. ...
    https://medlineplus.gov/genetics/chromosome/x - Genetics
  4. 15q11-q13 duplication syndrome 
    ... duplication of the genetic material. Dup15q syndrome Duplication/inversion 15q11 ... CHROMOSOME 15q11-q13 DUPLICATION SYNDROME ...
    https://medlineplus.gov/.../condition/15q11-q13-duplication-syndrome - Genetics
  5. Koolen-de Vries syndrome 
    ... an extremely small percentage of parents with the inversion have a child affected by Koolen-de Vries syndrome. ... KOOLEN-DE VRIES SYNDROME; KDVS ...
    https://medlineplus.gov/genetics/condition/koolen-de-vries-syndrome - Genetics
  6. Chromosome 20 
    ... on PubMed Gilbert F. Disease genes and chromosomes: disease maps ... inherited from a paternal inversion (20)(p13q13.1): clinical report and review of ...
    https://medlineplus.gov/genetics/chromosome/20 - Genetics
  7. Chromosome 16 
    ... additional abnormalities seen in some infants with this disorder. Like FOXF1, ... these rearrangements is an inversion of a region of chromosome 16 (written as ...
    https://medlineplus.gov/genetics/chromosome/16 - Genetics
  8. Chromosome 17 
    ... Human Map View Gilbert F. Disease genes and chromosomes: disease maps of the human genome. Chromosome 17. Genet ... JA, Brunner HG, de Vries BB. A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism. Nat Genet. 2006 Sep;38(9):999- ...
    https://medlineplus.gov/genetics/chromosome/17 - Genetics
  9. Chromosome 8 
    ... and an inversion of a segment of the chromosome. An inversion involves the breakage of a chromosome in two ... of DNA is reversed and reinserted into the chromosome. People with inversion duplication 8p typically have severe intellectual disability, a ...
    https://medlineplus.gov/genetics/chromosome/8 - Genetics
  10. Core binding factor acute myeloid leukemia 
    ... of DNA is reversed and reinserted into the chromosome. The inversion involved in CBF-AML (written as inv(16)) leads to the fusion of two genes on chromosome 16, CBFB and MYH11. Less commonly, a translocation ...
    https://medlineplus.gov/...ore-binding-factor-acute-myeloid-leukemia - Genetics
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