Autosomal recessive Peters anomaly, typical facial appearance, failure to thrive, hydrocephalus, and other anomalies: further delineation of the Krause-Kivlin syndrome.

Source:http://linkedlifedata.com/resource/pubmed/id/1887847

Am. J. Med. Genet. 1991 Jul 1 40 1 34-40

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PMID
1887847