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Dive into the research topics of 'A heterozygous 4-bp deletion mutation in the Gsα gene (GNAS1) in a patient with albright hereditary osteodystrophy'. Together they form a unique fingerprint.- Sort by
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Lee S. Weinstein, Pablo V. Gejman, Philippe de Mazancourt, Nadine American, Allen M. Spiegel
Research output: Contribution to journal › Article › peer-review