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Digeorge Syndrome-Velocardiofacial Syndrome Complex 2

Known as: DGS2, DIGEORGE SYNDROME/VELOCARDIOFACIAL SYNDROME COMPLEX 2 
 
National Institutes of Health

Papers overview

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2019
2019
Two polysaccharides, DGS1 and DGS2, were obtained by solid-state fermentation (SSF) of Fusarium solani DO7, an endophytic fungus… Expand
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2017
2017
Reproductive barriers are commonly observed in both animals and plants, in which they maintain species integrity and contribute… Expand
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2014
2014
Motivated by the use of forward guidance, we propose a method to estimate DSGE models in which the central bank holds the policy… Expand
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2011
2011
GATA3 mutations cause HDR (hypoparathyroidism, sensorineural deafness, and renal dysplasia) syndrome and, consistent with the… Expand
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Highly Cited
2009
Highly Cited
2009
AIM to describe a family with later onset congenital central hypoventilation syndrome (LO-CCHS) and heterozygosity for a 24… Expand
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2009
2009
Currently, molecular biologic techniques achieve a great development in studies of soil samples. The objective of this research… Expand
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2009
2009
GATA3 gene encodes a transcription factor expressed during thymus, liver, kidney, adrenal gland, central and peripheral nervous… Expand
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2002
2002
Heart defects are among the most common congenital anomalies, occurring in approximately 1% of newborn populations.1 Conotruncal… Expand
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2002
2002
We report on a prenatally diagnosed four-month-old boy with DiGeorge-like phenotype and a deletion of chromosome 10pter --> 14… Expand
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1998
1998
DiGeorge syndrome (DGS) is a developmental field defect, characterised by absent/hypoplastic thymus and parathyroid, and… Expand
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