Chromosome 22q11.2 Deletion Syndrome Presenting as Adult Onset Hypoparathyroidism: Clues to Diagnosis from Dysmorphic Facial Features

Lignende værker

• A Novel PRKAR1A Mutation Identified in a Patient with Isolated Primary Pigmented Nodular Adrenocortical Disease
  af: Korpaisarn, Sira, et al.
  Udgivet: (2017)
• Congenital Heart Defects and Dysmorphic Facial Features in Patients Suspicious of 22q11.2 Deletion Syndrome in Southern Brazil
  af: Diniz, Bruna Lixinski, et al.
  Udgivet: (2020)
• Hypoparathyroidism and 22q11 deletion syndrome
  af: Taylor, S, et al.
  Udgivet: (2003)
• Schizophrenia and chromosomal deletions within 22q11.2.
  af: Lindsay, E A, et al.
  Udgivet: (1995)
• 22q11.2 deletion syndrome
  af: McDonald-McGinn, Donna M., et al.
  Udgivet: (2015)