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Results 1 - 10 of 15 for Complex chromosomal rearrangement
  1. Wolf-Hirschhorn syndrome 
    ... or sperm) or during early embryonic development. More complex chromosomal rearrangements can also occur as de novo events, which ...
    https://medlineplus.gov/genetics/condition/wolf-hirschhorn-syndrome - Genetics
  2. Chronic myeloid leukemia 
    ... the BCR-ABL1 fusion gene is created by complex rearrangements that involve other chromosomes in addition to chromosomes 9 and 22. These ...
    https://medlineplus.gov/genetics/condition/chronic-myeloid-leukemia - Genetics
  3. 1p36 deletion syndrome 
    ... include a section near the end of the chromosome. The remaining 21 percent have complex rearrangements of genetic material that involve this region.The ...
    https://medlineplus.gov/genetics/condition/1p36-deletion-syndrome - Genetics
  4. Core binding factor acute myeloid leukemia 
    ... for making the two pieces of a protein complex known as core binding factor ... Chromosomal rearrangements involving the RUNX1 or CBFB gene alter CBF, ...
    https://medlineplus.gov/...ore-binding-factor-acute-myeloid-leukemia - Genetics
  5. Jacobsen syndrome 
    ... parent. In these cases, the parent carries a chromosomal rearrangement called a balanced translocation, in which a segment ... who inherit an unbalanced translocation can have a chromosomal rearrangement with some missing genetic material and some extra ...
    https://medlineplus.gov/genetics/condition/jacobsen-syndrome - Genetics
  6. Miller-Dieker syndrome 
    ... parent. In these cases, the parent carries a chromosomal rearrangement called a balanced translocation, in which no genetic ... who inherit an unbalanced translocation can have a chromosomal rearrangement with extra or missing genetic material. Individuals with ...
    https://medlineplus.gov/genetics/condition/miller-dieker-syndrome - Genetics
  7. WAGR syndrome 
    ... signs and symptoms of the condition has a chromosomal rearrangement called a balanced translocation. In this rearrangement, a piece of chromosome 11 is relocated to another chromosome, but no ...
    https://medlineplus.gov/genetics/condition/wagr-syndrome - Genetics
  8. Prader-Willi syndrome 
    ... Willi syndrome can also be caused by a chromosomal rearrangement called a translocation, or by a genetic alteration or other change that abnormally turns off (inactivates) genes on the paternal chromosome 15.It appears likely that the characteristic features ...
    https://medlineplus.gov/genetics/condition/prader-willi-syndrome - Genetics
  9. Angelman syndrome 
    ... Angelman syndrome can also be caused by a chromosomal rearrangement called a translocation, or by a variant or other defect in the region of DNA that controls activation of the UBE3A ... maternal copy of chromosome 15.The causes of Angelman syndrome are unknown ...
    https://medlineplus.gov/genetics/condition/angelman-syndrome - Genetics
  10. Recombinant 8 syndrome 
    ... found. Recombinant 8 syndrome is caused by a rearrangement of chromosome 8 that results in a deletion of a ... C, Maxwell JR. Postnatal diagnosis of de novo complex der(8) in a boy with prenatal diagnosis of recombinant chromosome 8 syndrome. Clin Case Rep. 2019 Mar 25; ...
    https://medlineplus.gov/genetics/condition/recombinant-8-syndrome - Genetics
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