Masayo Kagami
0000-0003-3020-455X
70 papers found
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Epimutation (hypomethylation) affecting the chromosome 14q32.2 imprinted region in a girl with upd(14)mat-like phenotype
Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes
Role of retrotransposon-derived imprinted gene, Rtl1, in the feto-maternal interface of mouse placenta
Placental hypoplasia in maternal uniparental disomy for chromosome 7
Molecular Mechanisms Leading to the Phenotypic Development in Paternal and Maternal Uniparental Disomy for Chromosome 14
Silver-Russell syndrome in a girl born after in vitro fertilization: partial hypermethylation at the differentially methylated region of PEG1/MEST
Target Height and Target Range for Japanese Children: Revisited
Segmental and full paternal isodisomy for chromosome 14 in three patients: Narrowing the critical region and implication for the clinical features
Clinical Assessment and Mutation Analysis of Kallmann Syndrome 1 (KAL1) and Fibroblast Growth Factor Receptor 1 (FGFR1, orKAL2) in Five Families and 18 Sporadic Patients
Analysis of the AAAS Gene in a Japanese Patient with Triple A Syndrome.
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