All Stories

  1. Expanding the genotype-phenotype spectrum of autosomal recessive Charcot-Marie-Tooth disease: A novel PLEKHG5 gene mutation
  2. A new familial case of Jalili syndrome caused by a novel mutation in CNNM4
  3. Lumbosacral spina bifida in a case with Pallister-Killian syndrome
  4. A novel mutated sequence in the T-box transcription factor-5 (TBX-5) gene (c.241A>T) in Holt–Oram syndrome
  5. Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease
  6. Severe Insulin Resistance Alters Metabolism in Mesenchymal Progenitor Cells
  7. The unprecedented recurrent diploid/tetraploid mosaicism of trisomy-18 (mixoploidy; 4n+18/2n+18): Clinical report
  8. Investigation of androgen receptor gene mutations in a series of 21 patients with 46,XY disorders of sex development
  9. ADAMTS4 and ADAMTS5 Knockout Mice Are Protected from Versican but Not Aggrecan or Brevican Proteolysis during Spinal Cord Injury
  10. ADAMTS1, ADAMTS5, ADAMTS9 and aggrecanase-generated proteoglycan fragments are induced following spinal cord injury in mouse
  11. A potential association between the number of CA repeats in the promoter region of the ADAMTS9 gene with lymphatic metastasis of breast cancer