Similar frequency of paternal uniparental disomy involving chromosome 20q (patUPD20q) in Japanese and Caucasian patients affected by sporadic pseudohypoparathyroidism type Ib (sporPHP1B)

समान संसाधन

• Segmental Paternal Uniparental Disomy (patUPD) of 14q32 With Abnormal Methylation Elicits the Characteristic Features of Complete patUPD14
  द्वारा: Irving, Melita D., और अन्य
  प्रकाशित: (2010)
• Paternal Uniparental Isodisomy of the Entire Chromosome 20 as a Molecular Cause of Pseudohypoparathyroidism Type Ib (PHP-Ib)
  द्वारा: Bastepe, Murat, और अन्य
  प्रकाशित: (2010)
• TSH elevations as the first laboratory evidence for pseudohypoparathyroidism type Ib (PHP-Ib)()
  द्वारा: Molinaro, Angelo, और अन्य
  प्रकाशित: (2015)
• Cytogenetic contribution to uniparental disomy (UPD)
  द्वारा: Liehr, Thomas
  प्रकाशित: (2010)
• Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients
  द्वारा: Eggermann, T., और अन्य
  प्रकाशित: (2001)