Is p57KIP2 mutation a common mechanism for Beckwith-Wiedemann syndrome or somatic overgrowth?
about
Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlationGenomic imprinting: concept and clinical consequences.Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways.Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.Analysis of CDKN1C in Beckwith Wiedemann syndrome.
P2860
Is p57KIP2 mutation a common mechanism for Beckwith-Wiedemann syndrome or somatic overgrowth?
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
Is p57KIP2 mutation a common m ...... yndrome or somatic overgrowth?
@en
type
label
Is p57KIP2 mutation a common m ...... yndrome or somatic overgrowth?
@en
prefLabel
Is p57KIP2 mutation a common m ...... yndrome or somatic overgrowth?
@en
P2093
P2860
P356
P1476
Is p57KIP2 mutation a common m ...... yndrome or somatic overgrowth?
@en
P2093
Friedrich U
Morison IM
Tommerup N
Wiedemann HR
P2860
P356
10.1136/JMG.35.1.86
P407
P577
1998-01-01T00:00:00Z