Molecular mechanisms leading to the phenotypic development in paternal and maternal uniparental disomy for chromosome 14

Clinical Pediatric Endocrinology

Volumn 17, Issue 4, 2008, Pages 103-111

  Ogata, Tsutomu ^a   Kagami, Masayo ^a  

^a NATIONAL RESEARCH INSTITUTE FOR CHILD HEALTH AND DEVELOPMENT   (Japan)

Author keywords

Chromosome 14; DMR; Epimutation; Imprinting; Uniparental disomy

Indexed keywords

CHROMOSOME 12; CHROMOSOME 14; DLK1 GENE; FATHER; GENE; GENE DELETION; GENE EXPRESSION; GENE SWITCHING; GENOTYPE; GTL2 GENE; HUMAN; HYPOTHESIS; KNOCKOUT MOUSE; KNOWLEDGE; METHYLATION; MOLECULAR MECHANICS; MOTHER; NONHUMAN; PHENOTYPE; PLACENTA; REVIEW; RTL1 GENE; UNIPARENTAL DISOMY;

EID: 56049096991     PISSN: 09185739     EISSN: 13477358     Source Type: Journal    
DOI: 10.1297/cpe.17.103     Document Type: Review

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