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K Kutyna

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Developmental Genetics|May 14, 1999
Genetic variation in trophectoderm function in parthenogenetic mouse embryosK E Latham, K Kutyna, Q Wang
Diabetes|June 28, 2000
Molecular basis and characterization of the hyperinsulinism/hyperammonemia syndrome: predominance of mutations in exons 11 and 12 of the glutamate dehydrogenase gene. HI/HA Contributing InvestigatorsC A Stanley, J Fang, K Kutyna, et al.
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Showing results (1-10 of 2) with videos related to

Sort By:
Pageof 1
Developmental Genetics|May 14, 1999
Genetic variation in trophectoderm function in parthenogenetic mouse embryosK E Latham, K Kutyna, Q Wang
Diabetes|June 28, 2000
Molecular basis and characterization of the hyperinsulinism/hyperammonemia syndrome: predominance of mutations in exons 11 and 12 of the glutamate dehydrogenase gene. HI/HA Contributing InvestigatorsC A Stanley, J Fang, K Kutyna, et al.
Pageof 1