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Results 1 - 10 of 39 for WHO
  1. ... service that provides information and support to people who have, or may be at risk for, genetic ... genetic condition. Genetics professionals include medical geneticists (doctors who specialize in genetics) and genetic counselors (certified healthcare ...
  2. ... testing are the purpose of the test and who receives the results. The goals of research testing ...
  3. ... disorders are more likely to occur among people who trace their ancestry to a particular geographic area. ...
  4. ... different from everyone else’s. Even identical twins, who have the same DNA, have different fingerprints. Few ...
  5. ... in genes on the X chromosome . In males (who have only one X chromosome), a variant in ... in each cell causes the disorder. In females (who have two X chromosomes), a variant in one ...
  6. ... own children. Autosomal recessive inheritance: Two unaffected people who each carry one copy of the altered gene ... with each pregnancy of having an unaffected child who is a carrier of the disorder is 50 ...
  7. ... testing Carrier testing is used to identify people who carry one copy of a gene mutation that, ... This type of testing is offered to individuals who have a family history of a genetic disorder ...
  8. ... an individual is raised. Studies of identical twins (who share 100 percent of their DNA) and their non-twin siblings (who share about 50 percent of their DNA) show ...
  9. Individuals or families who are concerned about an inherited condition may benefit from a genetic consultation. The reasons that a person might be ... pregnancy losses (miscarriages), a stillbirth, or a baby who died. A child with a known inherited disorder, ...
  10. ... the number of people in a specified group who develop a variant or disorder during a particular ... in a specified group at a given time who are living with the variant or disorder. This ...
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