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A single base pair mutation encoding a premature stop codon in the MIS type II receptor is responsible for canine persistent M?llerian duct syndrome.
Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 14-2002. A 51-year-old woman with recurrent hemoptysis.
Hemangiopericytoma
High-resolution crystallographic analysis of a co-operative dimeric hemoglobin.
Sequence specificity of streptozotocin-induced mutations.
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Sequence specificity of streptozotocin-induced mutations.
Mack SL, Fram RJ, Marinus MG. Sequence specificity of streptozotocin-induced mutations. Nucleic Acids Res. 1988 Oct 25; 16(20):9811-20.
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PubMed
subject areas
Base Sequence
Coliphages
DNA Mutational Analysis
Methylnitronitrosoguanidine
Mutation
Streptozocin
Tetracycline Resistance
authors with profiles
Martin G Marinus PHD