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Results 1 - 10 of 22 for most
  1. Chromosome 17 
    ... even among affected members of the same family.Most people with 17q12 deletion syndrome are missing about ... of DNA at 17q12.The segment that is most often deleted in people with 17q12 deletion syndrome ...
    https://medlineplus.gov/genetics/chromosome/17 - Genetics
  2. Mitochondrial DNA 
    ... fluid that surrounds the nucleus (the cytoplasm). Although most DNA is packaged in chromosomes within the nucleus, ... c oxidase deficiency. More About This Health Condition Most people with Kearns-Sayre syndrome have a single, ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics
  3. Chromosome 22 
    ... and mental illness such as schizophrenia (described below). Most people with 22q11.2 deletion syndrome are missing ... at position q11.2 on chromosome 22. In most cases, this extra genetic material consists of a ...
    https://medlineplus.gov/genetics/chromosome/22 - Genetics
  4. Chromosome 16 
    ... deletion also have an increased risk of seizures. Most people with the deletion have some of these ... rearrangements of genetic material on chromosome 16. The most common of these rearrangements is an inversion of ...
    https://medlineplus.gov/genetics/chromosome/16 - Genetics
  5. Chromosome 4 
    ... facioscapulohumeral muscular dystrophy type 2 (FSHD2), hypomethylation is most often a result of variants (also called mutations) ... keeps the DUX4 gene turned off (silenced) in most adult cells and tissues. In people with facioscapulohumeral ...
    https://medlineplus.gov/genetics/chromosome/4 - Genetics
  6. Chromosome 15 
    ... results from a phenomenon called genomic imprinting. The most common chromosome abnormality that leads to 15q11.2- ... the chromosome at a position designated q13.3. Most people with a 15q13.3 microdeletion are missing ...
    https://medlineplus.gov/genetics/chromosome/15 - Genetics
  7. Chromosome 1 
    ... of chromosome 1 is deleted in each cell. Most commonly, affected individuals are missing about 1.35 ... 1 region of chromosome 1 is involved in most cases of thrombocytopenia-absent radius (TAR) syndrome. TAR ...
    https://medlineplus.gov/genetics/chromosome/1 - Genetics
  8. Chromosome 3 
    ... very mild or no related signs and symptoms.Most people with 3q29 microdeletion syndrome are missing about ... of DNA at 3q29.The segment that is most often deleted in people with 3q29 microdeletion syndrome ...
    https://medlineplus.gov/genetics/chromosome/3 - Genetics
  9. Chromosome 5 
    ... blood cancer known as acute myeloid leukemia (AML).Most people with 5q- syndrome are missing a sequence ... these genes, PURA, is thought to lead to most of the characteristic features of the condition.The ...
    https://medlineplus.gov/genetics/chromosome/5 - Genetics
  10. Chromosome 12 
    ... eosinophils, a type of white blood cell. The most common translocation that causes this condition fuses part ... up of fatty tissue. In these tumors, the most common chromosome 12 rearrangements involve the long (q) ...
    https://medlineplus.gov/genetics/chromosome/12 - Genetics
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