Siegel-Bartlet J. et al "Craniofacial anomalies, cataracts, congenital heart disease, sacral neural tube defects, and growth and developmental retardation in two sisters: a new autosomal recessive MCA/MR syndrome?"   J Med Genet. 2002 Feb;39(2):145-8
Morgan NV. "A novel locus for Meckel-Gruber syndrome, MKS3, maps to chromosome 8q24"   Hum Genet. 2002 Oct;111(4-5):456-61
Smith UM. "The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat"   Nat Genet. 2006 Feb;38(2):191-6
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