19p13.12

A chromosome band present on 19p
National Institutes of Health

Topic mentions per year

Topic mentions per year

1995-2018
02419952018

Papers overview

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2013
2013
BACKGROUND The exstrophy-epispadias complex (BEEC) is a urogenital birth defect of varying severity. The causes of the BEEC are… (More)
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2013
2013
Dystonia type 4 (DYT4) was first described in a large family from Heacham in Norfolk with an autosomal dominantly inherited… (More)
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Highly Cited
2012
Highly Cited
2012
Transforming growth factor-β (TGF-β)-induced epithelial-mesenchymal transition (EMT) has been shown to be related to… (More)
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Highly Cited
2010
Highly Cited
2010
Triple negative breast cancers (TNBCs) have a relatively poor prognosis and cannot be effectively treated with current targeted… (More)
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Highly Cited
2010
Highly Cited
2010
Hereditary persistence of fetal hemoglobin (HPFH) is characterized by persistent high levels of fetal hemoglobin (HbF) in adults… (More)
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2010
2010
We describe the detailed clinical and molecular characterization of three patients (aged 7, 84/12 and 31 years) with overlapping… (More)
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2010
2010
We present a moderately mentally retarded boy with obesity, short stature, hypertrichosis and facial dysmorphism due to a… (More)
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2009
2009
We describe a patient with multiple congenital anomalies including deafness, lacrimal duct stenosis, strabismus, bilateral… (More)
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2006
2006
BACKGROUND The molecular basis of autosomal recessive non-syndromic mental retardation (NSMR) is poorly understood, mostly owing… (More)
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1995
1995
CD97 is a monomeric glycoprotein of 75 to 85 kDa that is induced rapidly on the surface of most leukocytes upon activation. We… (More)
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