Precocious Sister Chromatid Separation (PSCS) in Cornelia de Lange Syndrome

Những quyển sách tương tự

• NIPBL Mutational Analysis in 120 Individuals with Cornelia de Lange Syndrome and Evaluation of Genotype-Phenotype Correlations
  Bằng: Gillis, Lynette A., et al.
  Được phát hành: (2004)
• Chromosome Rearrangements in Cornelia de Lange Syndrome (CdLS): Report of a der(3)t(3;12)(p25.3;p13.3) in Two Half Sibs With Features of CdLS and Review of Reported CdLS Cases With Chromosome Rearrangements
  Bằng: DeScipio, Cheryl, et al.
  Được phát hành: (2005)
• Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B
  Bằng: Krantz, Ian D, et al.
  Được phát hành: (2004)
• The Incidence of Thrombocytopenia in Children with Cornelia de Lange Syndrome
  Bằng: Lambert, Michele P., et al.
  Được phát hành: (2010)
• Congenital Heart Disease in Cornelia de Lange Syndrome: Phenotype and Genotype Analysis
  Bằng: Chatfield, Kathryn C., et al.
  Được phát hành: (2012)