Multiple de novo copy number variations in two subjects with developmental problems and multiple congenital anomalies

פריטים דומים

• An organismal CNV mutator phenotype restricted to early human development
  מאת: Liu, Pengfei, et al.
  יצא לאור: (2017)
• Uncommon Deletions of the Smith-Magenis Syndrome Region Can Be Recurrent When Alternate Low-Copy Repeats Act as Homologous Recombination Substrates
  מאת: Shaw, Christine J., et al.
  יצא לאור: (2004)
• Copy Number Variation in Human Health, Disease, and Evolution
  מאת: Zhang, Feng, et al.
  יצא לאור: (2009)
• Detection and Inheritance Pattern of Copy Number Variations (CNVs) in Children with Multiple Congenital Anomalies
  מאת: Sheth, Frenny
  יצא לאור: (2014)
• De novo vs. inherited copy number variations in multiple sclerosis susceptibility
  מאת: Tizaoui, Kalthoum
  יצא לאור: (2018)