Mowat-Wilson syndrome in a fetus with antenatal diagnosis of short corpus callosum: advocacy for standard autopsy.
about
Neuroimaging Findings in Pediatric Genetic Skeletal Disorders: A Review.Experience of Mowat-Wilson syndrome prenatal diagnosis for a Chinese family.Retrospective analysis of prenatal ultrasound of children with Hirschsprung disease.Recurrent structural malformations identified among Mowat-Wilson syndrome fetuses.TGF-β1, Ghrelin, Neurexin, and Neuroligin are predictive biomarkers for postoperative prognosis of laparoscopic surgery in children with Hirschsprung disease.Polymicrogyria in a 10-month-old boy with Mowat-Wilson syndrome.
P2860
Mowat-Wilson syndrome in a fetus with antenatal diagnosis of short corpus callosum: advocacy for standard autopsy.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
Mowat-Wilson syndrome in a fet ...... advocacy for standard autopsy.
@en
type
label
Mowat-Wilson syndrome in a fet ...... advocacy for standard autopsy.
@en
prefLabel
Mowat-Wilson syndrome in a fet ...... advocacy for standard autopsy.
@en
P2093
P1476
Mowat-Wilson syndrome in a fet ...... advocacy for standard autopsy
@en
P2093
Anne-Lise Delezoide
Clarisse Baumann
Céline Dupont
Emmanuel Spaggiari
Fabien Guimiot
Jean-François Oury
Nadia Belarbi
P304
P356
10.1016/J.EJMG.2013.03.003
P577
2013-03-21T00:00:00Z