European guidance for the molecular diagnosis of pseudohypoparathyroidism not caused by point genetic variants at GNAS: an EQA study

समान संसाधन

• European guidance for the molecular diagnosis of pseudohypoparathyroidism not caused by point genetic variants at GNAS: an EQA study
  द्वारा: Garin, Intza, और अन्य
  प्रकाशित: (2015)
• Genome-wide DNA methylation analysis of pseudohypoparathyroidism patients with GNAS imprinting defects
  द्वारा: Rochtus, Anne, और अन्य
  प्रकाशित: (2016)
• Clinical utility gene card for: Pseudohypoparathyroidism
  द्वारा: Mantovani, Giovanna, और अन्य
  प्रकाशित: (2013)
• What to consider when pseudohypoparathyroidism is ruled out: iPPSD and differential diagnosis
  द्वारा: Pereda, Arrate, और अन्य
  प्रकाशित: (2018)
• 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
  द्वारा: Fernandez-Rebollo, Eduardo, और अन्य
  प्रकाशित: (2010)