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Results 1 - 10 of 25 for 3s -"3,4-Di-N-Hexanoyloxybutyl-1-Phosphocholine"
  1. Chromosome 3 
    ... divided into 23 pairs. Two copies of chromosome 3, one copy inherited from each parent, form one of the pairs. Chromosome 3 spans about 198 million base pairs (the building ...
    https://medlineplus.gov/genetics/chromosome/3 - Genetics
  2. Chromosome 16 
    ... DNA building blocks (base pairs) and represents almost 3 percent of the total DNA in cells.Identifying ... Rubinstein-Taybi syndrome (sometimes known as chromosome 16p13.3 deletion syndrome) have resulted from a deletion of ...
    https://medlineplus.gov/genetics/chromosome/16 - Genetics
  3. Chromosome 15 
    ... DNA building blocks (nucleotides) and represents more than 3 percent of the total DNA in cells.Researchers ... 15. More About This Health Condition A 15q13.3 microdeletion is a chromosomal change in which a ...
    https://medlineplus.gov/genetics/chromosome/15 - Genetics
  4. Chromosome 14 
    ... DNA building blocks (base pairs) and represents about 3.5 percent of the total DNA in cells. ... the human genome. Chromosome 14. Genet Test. 1999;3(4):379-91. doi: 10.1089/gte.1999. ...
    https://medlineplus.gov/genetics/chromosome/14 - Genetics
  5. Chromosome 17 
    ... base pairs) and represents between 2.5 and 3 percent of the total DNA in cells.Identifying ... of affected individuals, the duplicated segment is approximately 3.7 Mb in size. (A missing copy of ...
    https://medlineplus.gov/genetics/chromosome/17 - Genetics
  6. Chromosome 13 
    ... DNA building blocks (base pairs) and represents between 3.5 and 4 percent of the total DNA ... chromosome 13. These changes are known as 13q31.3 microdeletions. Feingold syndrome type 2 is characterized by ...
    https://medlineplus.gov/genetics/chromosome/13 - Genetics
  7. Chromosome 9 
    ... or number of copies of chromosome 9. 9q22.3 microdeletion is a chromosomal change in which a ... written as 352 kilobases (kb), in the q22.3 region of chromosome 9. This 352-kb segment ...
    https://medlineplus.gov/genetics/chromosome/9 - Genetics
  8. Chromosome 22 
    ... with 22q11.2 deletion syndrome are missing about 3 million base pairs on one copy of chromosome ... genetic material consists of a sequence of about 3 million base pairs, also written as 3 megabases ( ...
    https://medlineplus.gov/genetics/chromosome/22 - Genetics
  9. Chromosome 5 
    ... of AML. More About This Health Condition 5q31.3 microdeletion syndrome is caused by a chromosomal change ... of the chromosome at a position designated q31.3. The size of the deletion can range from ...
    https://medlineplus.gov/genetics/chromosome/5 - Genetics
  10. Chromosome 2 
    ... translocation) of genetic material between chromosomes 2 and 3 has been associated with cancers of a certain ... RC. Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key ...
    https://medlineplus.gov/genetics/chromosome/2 - Genetics
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