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4q25-q27

A chromosome band present on 4q
National Institutes of Health

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4 relations
ANK2 wt AlleleChromosomesFGF2 wt AllelePITX2 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Clinical utility gene card for: Long-QT Syndrome (types 1–13)
1.3 Name of the analysed genes or DNA/chromosome segments LQT1: KCNQ1, 11p15.5; LQT2: KCNH2, 7q35-q36; LQT3: SCN5A, 3p21; LQT4… 
Review
2003
Review
2003
A new case of an interstitial deletion (4)(q25q27) characterised by molecular cytogenetic techniques and review of the literature
Interstitial deletions of the long arm of chromosome 4 involving the region 4q25-q27 are rare. Clinical features of patients… 
2001
2001
Analysis of genetic alterations in salivary gland tumors by comparative genomic hybridization.
Highly Cited
2000
Highly Cited
2000
A Novel B Lymphocyte–Associated Adaptor Protein, Bam32, Regulates Antigen Receptor Signaling Downstream of Phosphatidylinositol 3-Kinase
We have identified and characterized a novel src homology 2 (SH2) and pleckstrin homology (PH) domain–containing adaptor protein… 
Highly Cited
1998
Highly Cited
1998
Construction and analysis of a sequence-ready map in 4q25: Rieger syndrome can be caused by haploinsufficiency of RIEG, but also by chromosome breaks approximately 90 kb upstream of this gene.
The autosomal dominant disorder Rieger syndrome (RIEG) shows genetic heterogeneity and has a phenotype characterized by… 
1997
1997
Rieger syndrome locus: a new reciprocal translocation t(4;12)(q25;q15) and a deletion del(4)(q25q27) both break between markers D4S2945 and D4S193.
Rieger syndrome (RS) is an autosomal dominant disorder of morphogenesis characterised by malformation of the anterior segment of… 
1996
1996
The linkage map of sheep Chromosome 6 compared with orthologous regions in other species
The genetic linkage map of sheep Chromosome (Chr) 6 has been extended to include 35 loci with the addition of 11 RFLP and 12… 
Review
1996
Review
1996
[Genetics of hereditary cardiopathies].
Hypertrophic cardiomyopathy may be secondary to a mutation in the cardiac beta myosin heavy chain (14q11-q12), alpha tropomyosin… 
1991
1991
Isolation and chromosomal localization of a novel nonerythroid ankyrin gene.
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