B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis

Author: Hopp Katharina   Heyer Christina M.   Hommerding Cynthia J.   Henke Susan A.   Sundsbak Jamie L.   Patel Shail   Patel Priyanka   Consugar Mark B.   Czarnecki Peter G.   Gliem Troy J.   Torres Vicente E.   Rossetti Sandro   Harris Peter C.  

Publisher: Oxford University Press

ISSN: 1460-2083

Source: Human Molecular Genetics, Vol.20, Iss.13, 2011-07, pp. : 2524-2534

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