Menkes disease complicated by concurrent Koolen-de Vries syndrome (17q21.31 deletion).

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Bibliographic Details
Title: Menkes disease complicated by concurrent Koolen-de Vries syndrome (17q21.31 deletion).
Authors: Woodfin T; Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama., Stoops C; Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama., Philips JB 3rd; Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama., Lose E; Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama., Mikhail FM; Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama., Hurst A; Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama.
Source: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2019 Aug; Vol. 7 (8), pp. e829. Date of Electronic Publication: 2019 Jun 28.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2324-9269 (Electronic) Linking ISSN: 23249269 NLM ISO Abbreviation: Mol Genet Genomic Med Subsets: MEDLINE
Database: MEDLINE Ultimate
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