An imprinted gene p57(KIP2) is mutated in Beckwith-Wiedemann syndrome

Nature Genetics

Volumn 14, Issue 2, 1996, Pages 171-173

  Hatada, I ^a   Ohashi, H ^a   Fukushima, Y ^a   Kaneko, Y ^a   Inoue, M ^a   Komoto, Y ^a   Okada, A ^a   Ohishi, S ^a   Nabetani, A ^a   Morisaki, H ^a   Nakayama, M ^a   Niikawa, N ^a   Mukai, T ^a  

^a NCCRI   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN P57; UNCLASSIFIED DRUG; CDKN1C PROTEIN, HUMAN; CYCLIN DEPENDENT KINASE INHIBITOR 1C; NUCLEAR PROTEIN;

ALLELISM; ARTICLE; BECKWITH WIEDEMANN SYNDROME; CELL PROLIFERATION; CONTROLLED STUDY; GENE LOCATION; GENE MUTATION; GENOME IMPRINTING; HUMAN; HUMAN CELL; MISSENSE MUTATION; PRIORITY JOURNAL; PROTEIN DOMAIN; CHILD; FEMALE; GENETICS; HETEROZYGOTE DETECTION; JAPAN; MALE; MUTATION; NEWBORN; NUCLEOTIDE SEQUENCE; TUMOR SUPPRESSOR GENE;

BECKWITH-WIEDEMANN SYNDROME; CHILD; CYCLIN-DEPENDENT KINASE INHIBITOR P57; DNA MUTATIONAL ANALYSIS; FEMALE; GENES, TUMOR SUPPRESSOR; GENOMIC IMPRINTING; HETEROZYGOTE DETECTION; HUMANS; INFANT, NEWBORN; JAPAN; MALE; MUTATION; NUCLEAR PROTEINS;

EID: 16044364516     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng1096-171     Document Type: Article

References (0)