Intragenic GNAS Deletion Involving Exon A/B in Pseudohypoparathyroidism Type 1A Resulting in an Apparent Loss of Exon A/B Methylation: Potential for Misdiagnosis of Pseudohypoparathyroidism Type 1B

Registos relacionados

• Intragenic GNAS Deletion Involving Exon A/B in Pseudohypoparathyroidism Type 1A Resulting in an Apparent Loss of Exon A/B Methylation: Potential for Misdiagnosis of Pseudohypoparathyroidism Type 1B
  Por: Fernandez-Rebollo, Eduardo, et al.
  Publicado em: (2010)
• Intragenic Deletions of GNAS in Pseudohypoparathyroidism Type 1A Identify a New Region Affecting Methylation of Exon A/B
  Por: Li, Dong, et al.
  Publicado em: (2020)
• Deletion of the Noncoding GNAS Antisense Transcript Causes Pseudohypoparathyroidism Type Ib and Biparental Defects of GNAS Methylation in cis
  Por: Chillambhi, Smitha, et al.
  Publicado em: (2010)
• What to consider when pseudohypoparathyroidism is ruled out: iPPSD and differential diagnosis
  Por: Pereda, Arrate, et al.
  Publicado em: (2018)
• Genome-wide DNA methylation analysis of pseudohypoparathyroidism patients with GNAS imprinting defects
  Por: Rochtus, Anne, et al.
  Publicado em: (2016)