The syndrome known as 16p11.2 deletion results from the absence of a fragment within a 220-kb area on chromosome 16 that is labeled as p11.2. This condition is associated with delays in development, cognitive impairment, and frequently, disorders within the autism spectrum.

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Chromosome 16p11.2 Deletion Syndrome, 220-KB

  • Parniyan Sadeghi,
  • Nima Rezaei

摘要

The syndrome known as 16p11.2 deletion results from the absence of a fragment within a 220-kb area on chromosome 16 that is labeled as p11.2. This condition is associated with delays in development, cognitive impairment, and frequently, disorders within the autism spectrum.