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Am J Med Genet. 1987 Sep;28(1):195-209.

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

Author information

1
Clinical Genetics Center Utrecht, The Netherlands.

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.

PMID:
3314510
DOI:
10.1002/ajmg.1320280127
[Indexed for MEDLINE]

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