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Acta Paediatr. 1993 Nov;82(11):993-6.

Silver-like syndrome and a small deletion on chromosome 13.

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  • 1Department of Clinical Genetics, East Hospital, Gothenburg, Sweden.

Abstract

A female child is described with features of Silver's syndrome, including pre- and postnatal growth delay, triangular face, hypertelorism, clinodactyly and developmental delay. In all lymphocytes analyzed, a small deletion was found in chromosome 13. The karyotype was 46,XX,del(13)(q22-32).

PMID:
8111185
[PubMed - indexed for MEDLINE]
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