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

Podobne zapisy

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