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Results 1 - 10 of 641 for Chromosome 7
  1. Chromosome 7 
    ... cell, divided into 23 pairs. Two copies of chromosome 7, one copy inherited from each parent, form one of the pairs. Chromosome 7 spans about 159 million DNA building blocks (base ...
    https://medlineplus.gov/genetics/chromosome/7 - Genetics
  2. CCM2 gene 
    ... scaffolding protein CCM2_HUMAN cerebral cavernous malformation 2 chromosome 7 open reading frame 22 MGC4067 MGC4607 OSM Tests ...
    https://medlineplus.gov/genetics/gene/ccm2 - Genetics
  3. MPLKIP gene 
    ... hair. More About This Health Condition ABHS C7orf11 chromosome 7 open reading frame 11 ORF20 TTD non-photosensitive ...
    https://medlineplus.gov/genetics/gene/mplkip - Genetics
  4. FOXP2-related speech and language disorder 
    ... a deletion that removes a small segment of chromosome 7, including the FOXP2 gene and several neighboring genes. ... results from a rearrangement of the structure of chromosome 7 (such as a translocation) or from inheriting two ...
    https://medlineplus.gov/...oxp2-related-speech-and-language-disorder - Genetics
  5. Russell-Silver syndrome 
    ... focused on genes located in particular regions of chromosome 7 and chromosome 11.People normally inherit one copy ... caused by a phenomenon called genomic imprinting. Both chromosome 7 and chromosome 11 contain groups of genes that ...
    https://medlineplus.gov/genetics/condition/russell-silver-syndrome - Genetics
  6. Williams syndrome 
    ... of genetic material from a specific region of chromosome 7. The deleted region includes 25 to 27 genes, ... presence or absence of the NCF1 gene on chromosome 7 impacts the risk of developing hypertension in people ...
    https://medlineplus.gov/genetics/condition/williams-syndrome - Genetics
  7. HOXA13 gene 
    ... rearrangements (translocations) involving the short (p) arm of chromosome 7 have been associated with leukemia, a cancer of ... forming cells. These translocations disrupt the region of chromosome 7 that contains several similar homeobox genes, including HOXA13. ...
    https://medlineplus.gov/genetics/gene/hoxa13 - Genetics
  8. FOXP2 gene 
    ... a deletion that removes a small segment of chromosome 7, including the FOXP2 gene and several neighboring genes. ... results from a rearrangement of the structure of chromosome 7 (such as a translocation) or from inheriting two ...
    https://medlineplus.gov/genetics/gene/foxp2 - Genetics
  9. 7q11.23 duplication syndrome 
    ... a region on the long (q) arm of chromosome 7 in each cell. This region is called the ... symptoms of 7q11.23 duplication syndrome. ELN GTF2I chromosome 7 7q11.23 duplication syndrome is considered to be ...
    https://medlineplus.gov/.../condition/7q1123-duplication-syndrome - Genetics
  10. Saethre-Chotzen syndrome 
    ... rearrangement of genetic material, in the region of chromosome 7 that contains the TWIST1 gene. When Saethre-Chotzen ... believe that a loss of other genes on chromosome 7 may be responsible for these additional features. TWIST1 ...
    https://medlineplus.gov/genetics/condition/saethre-chotzen-syndrome - Genetics
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