Publications by authors named "Gretel Beck"

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Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1).
Kirk Mykytyn, Darryl Y Nishimura, Charles C Searby, Gretel Beck, Kevin Bugge

Am J Hum Genet· February 2003

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Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia.
Roxanne Y Walder, Daniel Landau, Peter Meyer, Hanna Shalev, Maria Tsolia, Gretel E Beck

Nat Genet· June 2002

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