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Results 1 - 9 of 9 for neurological diseases
  1. Mitochondrial DNA 
    ... PubMed Dimauro S, Davidzon G. Mitochondrial DNA and disease. Ann Med. ... of Neurological Sciences. EFNS guidelines on the molecular diagnosis of ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics
  2. Chromosome 17 
    ... cases of a disorder called Charcot-Marie-Tooth disease. When this disorder is caused by changes affecting ... PMP22 gene, it is called Charcot-Marie-Tooth disease type 1A, or CMT1A. Charcot-Marie-Tooth disease ...
    https://medlineplus.gov/genetics/chromosome/17 - Genetics
  3. Chromosome 2 
    ... copies, has been found in myelodysplastic syndrome. This disease affects the blood and bone marrow. People with ...
    https://medlineplus.gov/genetics/chromosome/2 - Genetics
  4. Chromosome 16 
    ... Ensembl Human Map View: Chromosome 16 Gilbert F. Disease genes and chromosomes: disease maps of the human genome. Chromosome 16. Genet ...
    https://medlineplus.gov/genetics/chromosome/16 - Genetics
  5. Chromosome 15 
    ... on PubMed Ensembl Human Map View Gilbert F. Disease genes and chromosomes: disease maps of the human genome. Chromosome 15. Genet ...
    https://medlineplus.gov/genetics/chromosome/15 - Genetics
  6. Chromosome 1 
    ... a disorder called myelodysplastic syndrome, which is a disease of the blood and bone marrow. People with ...
    https://medlineplus.gov/genetics/chromosome/1 - Genetics
  7. Chromosome 5 
    ... U, List A, MacBeth KJ. Lenalidomide as a disease-modifying agent in patients with del(5q) myelodysplastic ...
    https://medlineplus.gov/genetics/chromosome/5 - Genetics
  8. Chromosome 7 
    ... is common in myelodysplastic syndrome, which is a disease of the blood and bone marrow. People with ...
    https://medlineplus.gov/genetics/chromosome/7 - Genetics
  9. X chromosome 
    ... Lyon MF. X-chromosome inactivation and human genetic disease. Acta Paediatr Suppl. 2002;91(439):107-12. ...
    https://medlineplus.gov/genetics/chromosome/x - Genetics