Diaphragmatic hernia-exomphalos-hypertelorism syndrome: A new case and further evidence of autosomal recessive inheritance

This publication has 2 references indexed in Scilit:

• Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: A newly recognized autosomal recessive disorder?
  American Journal of Medical Genetics, 1993
• Syndrome of ocular and facial anomalies, telecanthus, and deafness
  The Journal of Pediatrics, 1972