Isolated Growth Hormone Deficiency due to the R183H Mutation in GH1: Clinical Analysis of a Four-Generation Family

Ítems similars

• Pharmacokinetics of IGF-1 in PAPP-A2-Deficient Patients, Growth Response, and Effects on Glucose and Bone Density
  per: Cabrera-Salcedo, Catalina, et al.
  Publicat: (2017)
• MON-249 Algorithm-Driven Electronic Health Record Notification Enhances the Detection of Turner Syndrome
  per: Alexandrou, Eirene, et al.
  Publicat: (2019)
• Algorithm-Driven Electronic Health Record Notification Enhances the Detection of Turner Syndrome
  per: Alexandrou, Eirene, et al.
  Publicat: (2019)
• OR07-6 Integrating Targeted Bioinformatic Searches of the Electronic Health Records and Genomic Testing Identifies a Molecular Diagnosis in Three Patients with Undiagnosed Short Stature
  per: Cabrera Salcedo, Catalina, et al.
  Publicat: (2019)
• Nonclassical GH Insensitivity: Characterization of Mild Abnormalities of GH Action
  per: Storr, Helen L, et al.
  Publicat: (2018)