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1 se RNA of CYP79D1 and CYP79D2, Siritunga and Sayre obtained several lines with a reduction level vary
5 with three major clinical conditions: Kearns-Sayre syndrome, a multisystem disorder; Pearson syndrome
7 2,532-bp deletion of the type seen in Kearns-Sayre syndrome as well as a heteroplasmic A3243G mutatio
8 ost mtDNA-related diseases, including Kearns-Sayre syndrome, are recessive, only a few wild-type mtDN
9 A 35-year-old woman with features of Kearns-Sayre syndrome consisting of progressive ptosis, ophthal
10 ochondrial DNA (mtDNA) cause sporadic Kearns-Sayre syndrome, a fatal multisystem disorder, in which t
11 acterised by a complex phenotype; the Kearns-Sayre syndrome, for example, can include cardiac abnorma
12 itochondrial genomes of patients with Kearns-Sayre or Pearson syndromes, certain ophthalmic myopathie
15 o-dimensional basis was then extended by the Sayre equation into three dimensions by assigning a phas
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