Heterozygous Mutation within a Kinase-Conserved Motif of the Insulin-Like Growth Factor I Receptor Causes Intrauterine and Postnatal Growth Retardation

Παρόμοια τεκμήρια

• A Heterozygous Mutation of the Insulin-Like Growth Factor-I Receptor Causes Retention of the Nascent Protein in the Endoplasmic Reticulum and Results in Intrauterine and Postnatal Growth Retardation
  ανά: Wallborn, Tillmann, κ.ά.
  Έκδοση: (2010)
• Clinical and Functional Characterization of a Patient Carrying a Compound Heterozygous Pericentrin Mutation and a Heterozygous IGF1 Receptor Mutation
  ανά: Müller, Eva, κ.ά.
  Έκδοση: (2012)
• Spot urine iodine levels below the WHO recommendation are not related to impaired thyroid function in healthy children and adolescents
  ανά: Wallborn, Tillmann, κ.ά.
  Έκδοση: (2020)
• Concordance of bioactive vs. total immunoreactive serum leptin levels in children with severe early onset obesity
  ανά: Stanik, Juraj, κ.ά.
  Έκδοση: (2017)
• IGF1R Gene Alterations in Children Born Small for Gestitional Age (SGA)
  ανά: Janchevska, Aleksandra, κ.ά.
  Έκδοση: (2018)