Pseudohypoparathyroidism: phenotypic spectrum in kindred

समान संसाधन

• Congenital adrenal hypoplasia, glycerol kinase deficiency and myopathy: condition requiring prompt identification. Clinical and biochemical findings in two cases
  द्वारा: Vasanwala, Rashida, और अन्य
  प्रकाशित: (2013)
• Normocalcaemic pseudohypoparathyroidism with unusual phenotype.
  द्वारा: Gertner, J M, और अन्य
  प्रकाशित: (1978)
• Neuropsychiatric phenotype in a child with pseudohypoparathyroidism
  द्वारा: Visconti, Paola, और अन्य
  प्रकाशित: (2016)
• Right ventricular remodeling and dysfunction among the spectrum of heart failure phenotypes
  द्वारा: Wang, Harris, और अन्य
  प्रकाशित: (2016)
• Neonatal diabetes as an isolated manifestation of ipex: an expanding spectrum of disease phenotype with FOXP3 mutation
  द्वारा: Abraham, Mary, और अन्य
  प्रकाशित: (2015)