Further delineation of the 3‐M syndrome with review of the literature
- 1 September 1987
- journal article
- review article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 28 (1) , 195-209
- https://doi.org/10.1002/ajmg.1320280127
Abstract
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.Keywords
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