Further delineation of the 3-M syndrome with review of the literature.

@article{Hennekam1987FurtherDO,
  title={Further delineation of the 3-M syndrome with review of the literature.},
  author={Raoul C Hennekam and Jan B. Bijlsma and Juergen Spranger},
  journal={American journal of medical genetics},
  year={1987},
  volume={28 1},
  pages={195-209}
}
The 3-M syndrome is a clinically recognizable disorder characterized by prenatal and postnatal growth retardation and a spectrum of consistent minor anomalies. Intelligence seems normal. Inheritance is probably autosomal recessive, with possible expression of the mutant gene in the heterozygote. Three sibs with the 3-M syndrome are reported, together with an extensive review of the pertinent literature.