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Congenital omphalocele

Known as: Eventration, Exomphalos, Omphaloceles 
A congenital defect with major fissure in the ABDOMINAL WALL at the UMBILICUS resulting in the extrusion of VISCERA through the UMBILICUS. Unlike… Expand
National Institutes of Health

Papers overview

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Highly Cited
2008
Highly Cited
2008
The etiology of gastroschisis and omphalocele is unclear and their pathogenesis is controversial. Because previous reports have… Expand
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Highly Cited
2006
Highly Cited
2006
The type of vesicular transporter expressed by a neuron is thought to determine its neurotransmitter phenotype. We show that… Expand
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Highly Cited
2005
Highly Cited
2005
Rho-associated kinase (ROCK) I mediates signaling from Rho to the actin cytoskeleton. To investigate the in vivo functions of… Expand
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Highly Cited
2005
Highly Cited
2005
OBJECTIVES To assess at a population-based level the frequency with which severe structural congenital malformations are detected… Expand
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Highly Cited
2003
Highly Cited
2003
OBJECTIVE Several studies have shown an increased risk for neural tube defects associated with prepregnancy maternal obesity… Expand
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Highly Cited
2001
Highly Cited
2001
Podocalyxin is a CD34-related sialomucin that is expressed at high levels by podocytes, and also by mesothelial cells, vascular… Expand
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Highly Cited
2001
Highly Cited
2001
The presence of congenital malformations in infants born after IVF was studied from a register consisting of practically all… Expand
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Highly Cited
1997
Highly Cited
1997
In mice, the imprinted Igf2 gene (expressed from the paternal allele), which encodes a growth-promoting factor (IGF-II), is… Expand
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Highly Cited
1995
Highly Cited
1995
The MARCKS protein is a widely distributed cellular substrate for protein kinase C. It is a myristoylprotein that binds… Expand
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Highly Cited
1989
Highly Cited
1989
Of 253 infants with oesophageal atresia treated over an eight year period, 122 (48%) had a total of 213 other anomalies. Most… Expand
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