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   journal of clinical research in pediatric endocrinology   
سال:2016 - دوره:8 - شماره:Supplement 1


  tick  A case report of xp21 contiguous gene syndrome: Adrenal hypoplasia congenita,glycerol kinase deficiency,and duchenne muscular dystrophy - صفحه:14-15

  tick  A diabetic infant with homozygous LRBA mutation: The youngest patient reported - صفحه:16-

  tick  A novel missense mutation in hsd17b3 gene in two 46,xy siblings with female external gelitalia - صفحه:17-

  tick  Automating glycemic management in diabetes mellitus with a bionic pancreas - صفحه:4-

  tick  Congenital adrenal hyperplasia: Consensus guidelines and beyond - صفحه:12-13

  tick  Current perspectives on pseudohypoparathyroidism-new classification - صفحه:1-2

  tick  Disorders/differences of sex development: A world of uncertainty - صفحه:3-

  tick  Editorial

  tick  Efficacy and safety of long-acting gonadotropin releasing hormone analogs - صفحه:10-

  tick  Genetic defects affecting adrenal development - صفحه:11-

  tick  Idiopathic hypogonadotrophic hypogonadism caused by inactivating mutations in sra1 - صفحه:17-

  tick  Long-acting growth hormone formulations: Structure and activity - صفحه:6-

  tick  Premature pubarche,hyperinsulinemia,hypothyroxinemia and hyperintensities in basal ganglia: All caused by a single congenital defect - صفحه:14-

  tick  Pseudohypoparathyroisidm type 1a: A case report - صفحه:15-

  tick  The genetics of growth and growth disorders: From the hypothalamus to the epiphysis - صفحه:7-8

  tick  Turner syndrome: Care through the ages - صفحه:9-

  tick  Use of next generation sequencing in clinical practice: The example of disorders/differences of sex development - صفحه:5-
 

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