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  3. Research By Disease

Disease: Hypertelorism and tetralogy of Fallot

  • A Case Report of Donnai-Barrow Syndrome
  • A very rare case of a newborn with tetrasomy 9p and literature review
  • Autosomal recessive inheritance of a syndrome of hypertelorism, hypospadias, and tetralogy of Fallot?
  • Autosomal recessive tetralogy of Fallot, unusual facies, communicating hydrocephalus, and delayed language development: a new syndrome?
  • Cardiovascular dysplasia in Noonan's syndrome. Apropos of 64 cases
  • Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4
  • De novo inverted interstitial ("mirror") duplication of chromosome 8(q13----q24.1) in a liveborn male
  • Down syndrome: clinical profile from India
  • Facial and immunological anomalies associated with tetralogy of Fallot
  • Frontonasal dysplasia associated with tetralogy of Fallot
  • Frontonasal dysplasia, lipoma of the corpus callosum and tetralogy of Fallot
  • Molecular screening for 22Q11.2 deletion syndrome in patients with congenital heart disease
  • Natural history of mosaic trisomy 14 syndrome
  • Prenatal diagnosis of de novo terminal deletion of chromosome 7q
  • Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review
  • Teebi hypertelorism syndrome with tetralogy of Fallot
  • Trisomy 14 mosaicism in a 5-year-old boy
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