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4q21

A chromosome band present on 4q
National Institutes of Health

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13 relations
AFF1 wt AlleleCXCL1 wt AlleleCXCL10 wt AlleleCXCL13 wt Allele

Papers overview

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Review
2017
Review
2017
Amelogenesis Imperfecta in Children: Review of Pathogenetic Aspect
Amelogenesis imperfecta is an abnormal formation of the enamel. This anomaly associated with malformation of proteins, such as… 
2008
2008
Breakprone chromosome bands in lymphocytes from sarcoma patients do not coincide with bands involved in primary sarcoma-associated chromosome rearrangements.
The localization of breakpoints in spontaneous chromosome aberrations, i.e., chromatid and chromosome gaps, breaks, and exchanges… 
2005
2005
Assignment of cellular retinoic acid-binding protein 1 (CRABP1) and 2 (CRABP2) to porcine chromosome 7q12→q23 and 4q21→q23 by somatic cell and radiation hybrid panel mapping
CRABPs (cellular retinoic acid binding proteins) belong to members of a superfamily of lipid-binding proteins (Mansfield et al… 
2004
2004
Amelogenesis Imperfecta in a New Animal Model—a Mutation in Chromosome 5 (human 4q21)
Candidate genes for amelogenesis imperfecta (AI) and dentinogenesis imperfecta (DI) are located on 4q21 in humans. We tested our… 
Review
2004
Review
2004
Autosomal recessive and dominant polycystic kidney diseases.
It is possible to identify renal cysts in several subjects by ultrasonography imaging techniques. Among the inherited polycystic… 
2003
2003
The Chromosome 4 q 21 Gene ( AF-4 / FEL ) Is Widely Expressed in Normal Tissues and Shows Breakpoint Diversity in t ( 4 ; 1 l ) ( q 21 ; q 23 ) Acute Leukemia
The chromosomal translocation, t (4 ; l l )(q21 ;q23), is the most common type of 1 1 q23 chromosomal abnormality, being highly… 
2002
2002
Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers.
Autosomal dominant polycystic kidney disease (ADPKD), is an inherited disorder with genetic heterogeneity. The presence of renal… 
2002
2002
Hyper-IgE-syndrome
The hyper-IgE syndrome (HIES) is a rare primary immunodeficiency, characterized by eczema, elevated total IgE, and recurrent… 
1999
1999
Initial genome wide parametric genetic linkage analysis of schizophrenia and schizophrenia spectrum disorders finds lod scores above 3.00 on four chromosomes at 1Q22-23, 5Q22-35, 8P21-23 and 11Q14-24…
1986
1986
Correlations between immunological phenotype and karyotype in malignant lymphoma.
We have correlated immunological characteristics and karyotypic abnormalities from lymphomas in 118 patients. T-lymphomas… 
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