Assessing the Clinical Utility of SNP Microarray for Prader-Willi Syndrome due to Uniparental Disomy.

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Bibliographic Details
Title: Assessing the Clinical Utility of SNP Microarray for Prader-Willi Syndrome due to Uniparental Disomy.
Authors: Santoro SL; Division of Molecular and Human Genetics, Columbus, OH, USA., Hashimoto S, McKinney A, Mihalic Mosher T, Pyatt R, Reshmi SC, Astbury C, Hickey SE
Source: Cytogenetic and genome research [Cytogenet Genome Res] 2017; Vol. 152 (2), pp. 105-109. Date of Electronic Publication: 2017 Jul 27.
Publication Type: Journal Article
Journal Info: Publisher: S. Karger Country of Publication: Switzerland NLM ID: 101142708 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1424-859X (Electronic) Linking ISSN: 14248581 NLM ISO Abbreviation: Cytogenet Genome Res Subsets: MEDLINE
Database: MEDLINE Ultimate
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ISSN:1424-859X
DOI:10.1159/000478921