Figure 1: Overview and duplication content of human chromosome 15. Although the segmental duplications ... within the Prader-Willi/Angelman syndrome region) and aligned all duplicated regions ...

is associated with an abnormal phenotype (the central two are normal chromosome 15). d) The inv dup (22) (right) is associated with the cat eye syndrome.

Prader-Willi syndrome is a rare genetic disease that causes poor feeding in infancy but later triggers insatiable hunger.

While it might have given our ancestors an evolutionary advantage, an "unstable" region on human chromosome 15 is also the source ... to genetic recombination, duplication and other forms of ...

"Severe seizures occur in more than 80 percent of people with Angelman syndrome and Chromosome 15q duplication syndrome ... with Fragile X or Chromosome 15 Imprinting Disorders in Australia ...

New York, Aug. 26, 2020 (GLOBE NEWSWIRE) -- Reportlinker.com announces the release of the report "Dup15q Syndrome - Epidemiology Forecast - 2030" - https://www ...

gene on the chromosome X. MECP2 duplication syndrome primarily affects males, but females who carry the duplication on one X chromosome may exhibit some signs of the disorder. MECP2 is a rare ...

Prader-Willi syndrome is a genetic disorder caused by changes to chromosome 15. It affects growth, behavior, and learning and requires continual management to avoid potentially life threatening ...