Digeorge Syndrome-Velocardiofacial Syndrome Complex 2

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

Topic mentions per year

Topic mentions per year

1998-2017
0119982017

Papers overview

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2017
2017
Reproductive barriers are commonly observed in both animals and plants, in which they maintain species integrity and contribute… (More)
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2016
2016
Monosomy 10p is a rare chromosomal disorder with a prevalence <1/1,000,000, in which a terminal or interstitial distal region of… (More)
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2015
2015
The chromosome interval 10p15.3p14 harbors about a dozen genes. This region has been implicated in a few well-known human… (More)
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2011
2011
GATA3 mutations cause HDR (hypoparathyroidism, sensorineural deafness, and renal dysplasia) syndrome and, consistent with the… (More)
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2009
2009
Currently, molecular biologic techniques achieve a great development in studies of soil samples. The objective of this research… (More)
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2002
2002
Heart defects are among the most common congenital anomalies, occurring in approximately 1% of newborn populations. Conotruncal… (More)
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1998
1998
DiGeorge syndrome (DGS) is a developmental field defect, characterised by absent/hypoplastic thymus and parathyroid, and… (More)
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