Publications by authors named "Jennifer Ruth German"

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Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypes.
Soo-Jeong Kim, Jennifer L Miller, Paul J Kuipers, Jennifer Ruth German, Arthur L Beaudet

Eur J Hum Genet· March 2012

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A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes.
Marwan Shinawi, Christian P Schaaf, Samarth S Bhatt, Zhilian Xia, Ankita Patel, Jennifer Ruth German

Nat Genet· December 2009

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