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Results 1 - 10 of 1,409 for Have
  1. ... cut (cleaved) into smaller pieces called peptides that have different functions in the body. The peptides attach ( ... pain relief. Several mutations in the POMC gene have been found in people with proopiomelanocortin (POMC) deficiency. ...
  2. ... to a wide range of foreign invaders. Researchers have identified hundreds of different versions (alleles) of the ... specific combinations of HLA gene variants (HLA haplotypes) have been found to increase the risk of developing ...
  3. ... This Health Condition Variants in the FGFR3 gene have been found in approximately 30 percent of people ... of skin cells called keratinocytes. FGFR3 gene variants have not been found in people with other types ...
  4. ... variants (also called mutations) in the FGFR1 gene have been identified in people with encephalocraniocutaneous lipomatosis (ECCL), ... continue to grow and divide, some cells will have the variant and other cells will not. This ...
  5. ... At least ten mutations in the FGFR2 gene have been found to cause Apert syndrome. This condition ... facial features, and brain abnormalities. Affected individuals often have abnormalities of the fingers and toes, hearing and ...
  6. ... based on an individual's chromosomes. People usually have 46 chromosomes in each cell. Two of the ... or female sex characteristics. Girls and women typically have two X chromosomes (46,XX karyotype), while boys ...
  7. ... a nerve. DHH gene variants (also called mutations) have been identified in a small number of people ... a condition that affects sex development. Affected individuals have two altered copies of the DHH gene in ...
  8. ... region that allows muscles to stretch. Additionally, researchers have found that titin plays a role in chemical ... also known as mutations) in the TTN gene have been found to cause centronuclear myopathy, a condition ...
  9. ... More than 120 mutations in the SLC3A1 gene have been found to cause cystinuria. Many of these ... About This Health Condition Some people with cystinuria have large DNA deletions that remove not only the ...
  10. ... More than 100 mutations in the BEST1 gene have been identified in people with vitelliform macular dystrophy. ... ADVIRC); at least four mutations in this gene have been found in affected individuals. ADVIRC is characterized ...
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