Turner syndrome caused by rare complex structural abnormalities involving chromosome X

Lignende værker

• Clinical characteristics and follow-up of 5 young Chinese males with gonadotropin-releasing hormone deficiency caused by mutations in the KAL1 gene
  af: Li, Juan, et al.
  Udgivet: (2015)
• Down's/Turner's mosaicism. Double aneuploidy as a rare cause of missed prenatal diagnosis of chromosomal abnormality.
  af: MacFaul, R, et al.
  Udgivet: (1981)
• Causal variants screened by whole exome sequencing in a patient with maternal uniparental isodisomy of chromosome 10 and a complicated phenotype
  af: LI, NIU, et al.
  Udgivet: (2016)
• X-Chromosome Gene Dosage and the Risk of Diabetes in Turner Syndrome
  af: Bakalov, Vladimir K., et al.
  Udgivet: (2009)
• Rare X Chromosome Abnormalities in Systemic Lupus Erythematosus and Sjögren’s Syndrome
  af: Sharma, Rohan, et al.
  Udgivet: (2017)