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Publications by Kenji Kurosawa

Exploring the Unique Function of Imprinting Control Centers in the PWS/AS-responsible Region: Finding From Array-Based Methylation Analysis in Cases With Variously Sized Microdeletions

Clinical Epigenetics
GeneticsDevelopmental BiologyMolecular Biology
2019English

Comprehensive Clinical Studies in 34 Patients With Molecularly Defined UPD(14)pat and Related Conditions (Kagami–Ogata Syndrome)

European Journal of Human Genetics
Genetics
2015English

HRAS Mutants Identified in Costello Syndrome Patients Can Induce Cellular Senescence: Possible Implications for the Pathogenesis of Costello Syndrome

Journal of Human Genetics
Genetics
2011English

Diamond-Blackfan Anemia Caused by Chromosome 1p22 Deletion Encompassing RPL5

Human Genome Variation
BiochemistryGeneticsMolecular Biology
2019English

Novel CUL7 Biallelic Mutations Alter the Skeletal Phenotype of 3M Syndrome

Human Genome Variation
BiochemistryGeneticsMolecular Biology
2020English

Preferential Paternal Origin of Microdeletions Caused by Prezygotic Chromosome or Chromatid Rearrangements in Sotos Syndrome

American Journal of Human Genetics
Genetics
2003English

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