Clonal heterogeneity at allelic methylation sites diagnostic for Prader-Willi and Angelman syndromes.
about
Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients1031-1034delTAAC (Leu125Stop): a novel familial UBE3A mutation causing Angelman syndrome in two siblings showing distinct phenotypes.Age-dependent decrease and alternative splicing of methionine synthase mRNA in human cerebral cortex and an accelerated decrease in autismInfluence of in vitro manipulation on the stability of methylation patterns in the Snurf/Snrpn-imprinting region in mouse embryonic stem cells
P2860
Clonal heterogeneity at allelic methylation sites diagnostic for Prader-Willi and Angelman syndromes.
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
Clonal heterogeneity at alleli ...... -Willi and Angelman syndromes.
@ast
Clonal heterogeneity at alleli ...... -Willi and Angelman syndromes.
@en
type
label
Clonal heterogeneity at alleli ...... -Willi and Angelman syndromes.
@ast
Clonal heterogeneity at alleli ...... -Willi and Angelman syndromes.
@en
prefLabel
Clonal heterogeneity at alleli ...... -Willi and Angelman syndromes.
@ast
Clonal heterogeneity at alleli ...... -Willi and Angelman syndromes.
@en
P2093
P2860
P356
P1476
Clonal heterogeneity at alleli ...... -Willi and Angelman syndromes.
@en
P2093
P2860
P304
P356
10.1073/PNAS.95.4.1675
P407
P577
1998-02-01T00:00:00Z