All Stories

  1. Assessing Skewed X-Chromosome Inactivation
  2. Reorganization of inter‐ chromosomal interactions in the 2q37‐deletion syndrome
  3. Small Supernumerary Marker Chromosome May Provide Information on Dosage-insensitive Pericentric Regions in Human
  4. Molecular Cytogenetic Analysis of One African and Five Asian Macaque Species Reveals Identical Karyotypes as in Mandrill
  5. A Girl with 10 Mb Distal Xp Deletion Arising from Maternal Pericentric Inversion: Clinical Data and Molecular Characterization
  6. 7q11.23 microduplication syndrome: neurophysiological and neuroradiological insights into a rare chromosomal disorder
  7. Inactivation of AMMECR1 is associated with growth, bone, and heart alterations
  8. Next generation phenotyping in Emanuel and Pallister-Killian syndrome using computer-aided facial dysmorphology analysis of 2D photos
  9. Noninvasive Prenatal Testing - When Is It Advantageous to Apply
  10. First Molecular Cytogenetic Characterization of Murine Malignant Mesothelioma Cell Line AE17 and In Silico Translation to the Human Genome
  11. X-autosome and X-Y translocations in female carriers: X-chromosome inactivation easily detectable by 5-ethynyl-2-deoxyuridine (EdU)
  12. Interphase Molecular Cytogenetic Detection Rates of Chronic Lymphocytic Leukemia-Specific Aberrations Are Higher in Cultivated Cells Than in Blood or Bone Marrow Smears
  13. A New Case of a Complex Small Supernumerary Marker Chromosome: A Der(9)t(7;9)(p22;q22) due to a Maternal Balanced Rearrangement
  14. molecular cytogenetics in cancer diagnosi