about
Clinical and molecular phenotype of Aicardi-Goutieres syndromeMutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection.Pena-Shokeir phenotype (fetal akinesia deformation sequence) revisited.Intracranial calcification in childhood: a review of aetiologies and recognizable phenotypes.Less invasive autopsy: benefits and limitations of the use of magnetic resonance imaging in the perinatal postmortem.Recurrent pseudo-TORCH appearances of the brain presenting as "Dandy-Walker" malformation.
P2860
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Severe fetal brain dysgenesis with focal calcification.
@en
type
label
Severe fetal brain dysgenesis with focal calcification.
@en
prefLabel
Severe fetal brain dysgenesis with focal calcification.
@en
P2093
P356
P1433
P1476
Severe fetal brain dysgenesis with focal calcification
@en
P2093
Ian Simpson
R J McKinlay Gardner
Simon E Meagher
P304
P356
10.1002/PD.1152
P577
2005-05-01T00:00:00Z