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Deletion of the short arm of chromosome 3: a case report with necropsy findings.

A male infant with partial deletion of the short arm of chromosome 3 is described. The features this patient shares with six previously reported cases include microcephaly, dolichocephaly, micrognathia, epicanthic folds, ptosis, low set or malformed ears, postaxial polydactyly, and growth or mental...

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Bibliographic Details
Main Authors: Beneck, D, Suhrland, M J, Dicker, R, Greco, M A, Wolman, S R
Format: Artigo
Language:Inglês
Published: 1984
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Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1049304/
https://ncbi.nlm.nih.gov/pubmed/6492097
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