Deletion of the Noncoding GNAS Antisense Transcript Causes Pseudohypoparathyroidism Type Ib and Biparental Defects of GNAS Methylation in cis

Míreanna Comhchosúla

• Deletion of the Noncoding GNAS Antisense Transcript Causes Pseudohypoparathyroidism Type Ib and Biparental Defects of GNAS Methylation in cis
  le: Chillambhi, Smitha, et al.
  Foilsithe: (2010)
• A Novel STX16 Deletion in Autosomal Dominant Pseudohypoparathyroidism Type Ib Redefines the Boundaries of a cis-Acting Imprinting Control Element of GNAS
  le: Linglart, Agnès, et al.
  Foilsithe: (2005)
• De Novo STX16 Deletions: An Infrequent Cause of Pseudohypoparathyroidism Type Ib that Should Be Excluded in Sporadic Cases
  le: Turan, Serap, et al.
  Foilsithe: (2012)
• Recessive versus imprinted disorder: consanguinity can impede establishing the diagnosis of autosomal dominant pseudohypoparathyroidism type Ib
  le: Turan, Serap, et al.
  Foilsithe: (2010)
• GNAS AS2 methylation status enables mechanism-based categorization of pseudohypoparathyroidism type 1B
  le: Yorihiro Iwasaki, et al.
  Foilsithe: (2024-03-01)