about
Intragenic GNAS deletion involving exon A/B in pseudohypoparathyroidism type 1A resulting in an apparent loss of exon A/B methylation: potential for misdiagnosis of pseudohypoparathyroidism type 1BEvolution in health and medicine Sackler colloquium: Somatic evolutionary genomics: mutations during development cause highly variable genetic mosaicism with risk of cancer and neurodegeneration.Recent updates on genetics: teaching old dogmas new tricks.X-linked ichthyosis: differential diagnosis of low maternal oestriol level.
P2860
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh
2006年學術文章
@zh-hant
name
Mosaicism in genetic skin disorders.
@ast
Mosaicism in genetic skin disorders.
@en
type
label
Mosaicism in genetic skin disorders.
@ast
Mosaicism in genetic skin disorders.
@en
prefLabel
Mosaicism in genetic skin disorders.
@ast
Mosaicism in genetic skin disorders.
@en
P2860
P1476
Mosaicism in genetic skin disorders.
@en
P2093
Dawn H Siegel
Virginia P Sybert
P2860
P356
10.1111/J.1525-1470.2006.00180.X
P577
2006-01-01T00:00:00Z