Mandibulofacial Dysostosis

Known as: Mandibulofacial Dysostosis [Disease/Finding], TREACHER COLLINS SYNDROME, Mandibulofacial Dysostoses 
A hereditary disorder occurring in two forms: the complete form (Franceschetti's syndrome) is characterized by antimongoloid slant of the palpebral… (More)
National Institutes of Health

Papers overview

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2012
2012
Mandibulofacial dysostosis with microcephaly (MFDM) is a rare sporadic syndrome comprising craniofacial malformations… (More)
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Review
2010
Review
2010
Ribosomopathies compose a collection of disorders in which genetic abnormalities cause impaired ribosome biogenesis and function… (More)
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Highly Cited
2009
Highly Cited
2009
H geneticists seek to understand the inherited basis of human biology and disease, aiming either to gain insights that could… (More)
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Highly Cited
2008
Highly Cited
2008
Usually the reference genes used in gene expression analysis have been chosen for their known or suspected housekeeping roles… (More)
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Highly Cited
2005
Highly Cited
2005
Does media bias affect voting? We address this question by looking at the entry of Fox News in cable markets and its impact on… (More)
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Highly Cited
2000
Review
1995
Review
1995
Vascular endothelial cells, by virtue of their unique anatomical position, are constantly exposed to the fluid mechanical forces… (More)
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Highly Cited
1993
Highly Cited
1993
1. The silent period evoked in the first dorsal interosseous (FDI) muscle after electrical and magnetic transcranial stimulation… (More)
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1991
1991
Mandibulofacial dysostosis is an autosomal dominant malformation incorporating a number of facial and hearing defects. It has… (More)
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Highly Cited
1975
Highly Cited
1975
Numerous synonyms have been used to describe syndromes affecting structures derived from the first and second branchial arches… (More)
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