A supernumerary marker chromosome 15 tetrasomic for the Prader-Willi/Angelman syndrome critical region in a patient with a severe phenotype

Benzer Materyaller

• A patient with a supernumerary marker chromosome (15), Angelman syndrome, and uniparental disomy resulting from paternal meiosis II non-disjunction
  Yazar:: Roberts, S, ve diğerleri
  Baskı/Yayın Bilgisi: (2002)
• CHROMOSOME 15 IN PRADER‐WILLI SYNDROME
  Yazar:: Fear, C. N., ve diğerleri
  Baskı/Yayın Bilgisi: (2008)
• Copy neutral absence of heterozygosity on chromosome 15 distal long arm: A surrogate marker for Prader–Willi/Angelman syndromes?
  Yazar:: Ortega, Veronica, ve diğerleri
  Baskı/Yayın Bilgisi: (2021)
• Molecular and Fluorescence In Situ Hybridization Characterization of the Breakpoints in 46 Large Supernumerary Marker 15 Chromosomes Reveals an Unexpected Level of Complexity
  Yazar:: Roberts, S. E., ve diğerleri
  Baskı/Yayın Bilgisi: (2003)
• A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man.
  Yazar:: Crolla, J A, ve diğerleri
  Baskı/Yayın Bilgisi: (1992)