Is p57(KIP2) mutation a common mechanism for Beckwith-Wiedemann syndrome or somatic overgrowth? [6]

Journal of Medical Genetics

Volumn 35, Issue 1, 1998, Pages 86-

  Okamoto, K ^a   Morrison, I M ^a   Reeve, A E ^a   Tommerup, N ^a   Wiedemann, R ^a   Friedrich, U ^a  

^a UNIVERSITY OF OTAGO   (New Zealand)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; PROTEIN; CDKN1C PROTEIN, HUMAN; CYCLIN DEPENDENT KINASE INHIBITOR 1C; NUCLEAR PROTEIN;

BECKWITH WIEDEMANN SYNDROME; CHROMOSOME 11P; GENE DELETION; GENE MUTATION; GENOME IMPRINTING; GROWTH DISORDER; HUMAN; LETTER; NEPHROBLASTOMA; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; GENETICS; MUTATION;

BECKWITH-WIEDEMANN SYNDROME; CYCLIN-DEPENDENT KINASE INHIBITOR P57; GROWTH DISORDERS; HUMANS; MUTATION; NUCLEAR PROTEINS;

EID: 0031613188     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (20)