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3q27.3

A chromosome band present on 3q
National Institutes of Health

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Chromosomes

Papers overview

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2017
2017
Abstract 690: Identifying the genetic basis of stage 4S neuroblastoma
Introduction: The 5 year mortality rate for stage 4 metastatic neuroblastoma (NBL) is ~50%; however, the stage 4S subset of NBL… 
2016
2016
Frameshift Sequence Variants in the Human Lipase‐H Gene Causing Hypotrichosis
Hypotrichosis is a condition of abnormal hair pattern characterized by sparse to absent hair on different parts of the body… 
2015
2015
GWAS reveal novel IgA nephropathy risk loci
IgA nephropathy, also known as Berger's disease, is the most common primary glomerulonephritis and a major cause of end stage… 
2011
2011
Identification of LIPH gene mutation in a consanguineous family segregating the woolly hair/hypotrichosis phenotype.
OBJECTIVE To identify the disease causing gene in a four generation consanguineous family in which eleven family members were… 
2009
2009
A genome-wide scan for the Sasang constitution in a Korean family suggests significant linkage at chromosomes 8q11.22-23 and 11q22.1-3.
OBJECTIVES We aim to identify the genetic loci responsible for Sasang constitution type, which is important for effective… 
2007
2007
Somatostatin genetic variants modify the risk for Alzheimer's disease among Finnish patients
The levels of somatostatin are consistently decreased in the brain and cerebrospinal fluid of Alzheimer’s disease (AD) patients… 
Highly Cited
2005
Highly Cited
2005
Gamma-S crystallin gene (CRYGS) mutation causes dominant progressive cortical cataract in humans
Background: Congenital or childhood cataract is clinically and genetically a highly heterogeneous lens disorder in children… 
2003
2003
Omphalocele in trisomy 3q: further delineation of phenotype
We report a case of a patient with omphalocele, dysmorphic features, and mild developmental delay associated with a chromosomal… 
2002
2002
Genetic changes in uroepithelial tumors of patients with Balkan endemic nephropathy.
BACKGROUND Balkan endemic nephropathy (BEN) is seen in certain regions of the Balkan Peninsula. The patients are predisposed to… 
2002
2002
ASSOCIATION OF COMMON GENETIC VARIANTS OF XENOBIOTIC METABOLIZING ENZYMES ( CYPS AND GSTS ) WITH BALKAN ENDEMIC NEPHROPATHY : A STUDY IN THE VRATZA ' S DISTRICT OF BULGARIA
RENAL INTERSTITIAL FIBROSIS IS A MAJOR FEATURE OF BALKAN ENDEMIC NEPHROPATHY (BEN) G. A. Müller, M. Zeisberg, F Strutz Dept. of… 
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