Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/7137
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Type: Journal article
Title: A second case of microcephaly, microphthalmia, ectrodactyly (split foot), and prognathism (MMEP)
Author: Suthers, G.
Morris, L.
Citation: Clinical Dysmorphology, 1996; 5(1):77-79
Publisher: CHAPMAN HALL LTD
Issue Date: 1996
ISSN: 0962-8827
1473-5717
Abstract: In 1993, Viljoen and Smart described a woman with ectrodactyly of the feet, midline facial cleft, microphthalmia, and mental retardation in association with a de novo chromosome 6;13 translocation. We present a man with similar features who had a normal karyotype.
Keywords: Humans; Foot Deformities, Congenital; Prognathism; Microcephaly; Microphthalmos; Syndrome; Adult; Male
RMID: 0030005684
DOI: 10.1097/00019605-199601000-00012
Appears in Collections:Paediatrics publications

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