| Literature DB >> 10528239 |
J R Avansino1, T R Dennis, P Spallone, A D Stock, M L Levin.
Abstract
We describe an infant with trisomy of (5)(p10p13.1) resulting from a de novo marker chromosome. The marker's origin was identified by chromosome microdissection and reverse in situ hybridization. The clinical findings are compared to those of other partial and complete 5p duplications. This case further defines the critical region of 5p trisomy syndrome to proximal 5p. Copyright 1999 Wiley-Liss, Inc.Entities:
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Year: 1999 PMID: 10528239
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299