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Exome capture and massively parallel sequencing identifies a novel HPSE2 mutation in a Saudi Arabian child with Ochoa (urofacial) syndrome

✍ Scribed by Wisam Al Badr; Suha Al Bader; Edgar Otto; Friedhelm Hildebrandt; Todd Ackley; Weiping Peng; Jishu Xu; Jun Li; Kailey M. Owens; David Bloom; Jeffrey W. Innis


Book ID
116694263
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
545 KB
Volume
7
Category
Article
ISSN
1477-5131

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