All Stories

  1. Molecular characterisation of a case of dicentric Y presented as nonobstructive azoospermia with testicular early maturation arrest
  2. Disorder of Sex Development: Spectrum of Disorders in a Referral Tertiary Care Hospital in North India
  3. Lethal Developmental Defects: An Overview
  4. Disorder of Sex Development: Spectrum of Disorders in a Referral Tertiary Care Hospital in North India
  5. Suspected microdeletion syndromes and molecular cytogenetic techniques: an experience with 330 cases
  6. Dark-coloured semen in nonobstructive azoospermia: a report of four cases
  7. Rapid detection of chromosome X, Y, 13, 18, and 21 aneuploidies by primed in situ labeling/synthesis technique
  8. Chromosome 22q11.2 microdeletion in monozygotic twins with discordant phenotype and deletion size
  9. Prevalence of 22q11.2 microdeletion in 146 patients with cardiac malformation in a referral hospital of North India
  10. Amniotic band syndrome and/or limb body wall complex: split or lump
  11. Assessment of 1p/19q status by fluorescence in situ hybridization assay: A comparative study in oligodendroglial, mixed oligoastrocytic and astrocytic tumors
  12. Mosaic 22q11.2 microdeletion syndrome: diagnosis and clinical manifestations of two cases
  13. Iniencephaly and chromosome mosaicism: A report of two cases
  14. Placental chimerism in early human pregnancy
  15. Osteodysplastic primordial dwarfism type ii with normal intellect but delayed central nervous system myelination
  16. Detection of fetal cells in transcervical samples and prenatal diagnosis of chromosomal abnormalities
  17. Isolation of fetal cells from transcervical samples by micromanipulation: Molecular confirmation of their fetal origin and diagnosis of fetal aneuploidy
  18. OEIS complex with craniofacial anomalies—defect of blastogenesis?
  19. GAPO syndrome in a child without dermal hyaline deposit
  20. Preaxial brachydactyly with abduction of thumbs and hallux varus: A distinct entity