All Stories

  1. Impact of a novel 14 bp MEN1 deletion in a patient with hyperparathyroidism and gastrinoma
  2. Rare association of acromegaly with left atrial myxoma in Carney's complex due to novel PRKAR1A mutation
  3. Prospective Case–Control Study to Evaluate the Role of Glutathione S Transferases (GSTT1 and GSTM1) Gene Deletion in Breast Carcinoma and Its Prognostic Significance
  4. Assessment of fine needle aspiration cytology samples for molecular genetic analysis in neuroblastoma
  5. Loss of heterozygosity at 11p13 and 11p15 in Wilms tumor: a study of 22 cases from India
  6. Y Cell Line in a Turner Mosaic: A Case Report
  7. Molecular Genetic Analysis of Macular Corneal Dystrophy Patients from North India
  8. Molecular genetic analysis of CYP21A2 gene in patients with congenital adrenal hyperplasia
  9. Growth and hormonal profile from birth to adolescence of a girl with aromatase deficiency
  10. A Novel <i>TGFBI</i> Phenotype with Amyloid Deposits and Arg124Leu Mutation
  11. An unusual association of hypospadias with partial deletion of chromosome 1q
  12. Spinal Myxopapillary Ependymoma With Down Syndrome: Exploring an Unusual Association
  13. Cytogenetic evaluation of neuroblastoma using fine needle aspiration cultures
  14. Tetraploid mixoploidy presenting as refractory hydrops in a case of immune hemolytic anemia
  15. Microsatellite Variation at 24 STR Loci in Three Endogamous Groups of Uttar Pradesh, India