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Publications by Norio Niikawa
SMOC1 Is Essential for Ocular and Limb Development in Humans and Mice
American Journal of Human Genetics
Genetics
Loss of CpG Methylation Is Strongly Correlated With Loss of Histone H3 Lysine 9 Methylation at DMR-LIT1 in Patients With Beckwith-Wiedemann Syndrome
American Journal of Human Genetics
Genetics
Preferential Paternal Origin of Microdeletions Caused by Prezygotic Chromosome or Chromatid Rearrangements in Sotos Syndrome
American Journal of Human Genetics
Genetics
ASC, a Novel 22-kDa Protein, Aggregates During Apoptosis of Human Promyelocytic Leukemia HL-60 Cells
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Domain-Specific Mutations of a Transforming Growth Factor (TGF)-β1 Latency-Associated Peptide Cause Camurati-Engelmann Disease Because of the Formation of a Constitutively Active Form of TGF-β1
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Japanese and North American/European Patients With Beckwith–Wiedemann Syndrome Have Different Frequencies of Some Epigenetic and Genetic Alterations
European Journal of Human Genetics
Genetics
Microarray Comparative Genomic Hybridization Analysis of 59 Patients With Schizophrenia
Journal of Human Genetics
Genetics
Analysis of the NSD1 Promoter Region in Patients With a Sotos Syndrome Phenotype
Journal of Human Genetics
Genetics
Phenotype?genotype Correlation in Two Patients With 12q Proximal Deletion
Journal of Human Genetics
Genetics
Microarray Comparative Genomic Hybridization (CGH)-based Prenatal Diagnosis for Chromosome Abnormalities Using Cell-Free Fetal DNA in Amniotic Fluid
Journal of Human Genetics
Genetics
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