Skip to search formSkip to main contentSkip to account menu

2q37

A chromosome band present on 2q
National Institutes of Health

Related topics

Related topics

7 relations
ALPP wt AlleleChromosomesUGT1A LocusUGT1A1 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2011
2011
Exclusion of linkage to chromosomes 14q, 2q37 and 8p21.1-q11.23 in a Serbian family with idiopathic basal ganglia calcification
In this study we report clinical and imaging data from a multigenerational Serbian family with idiopathic basal ganglia… 
Review
2009
Review
2009
Bone morphogenetic protein-2 activity is regulated by secreted phosphoprotein-24 kd, an extracellular pseudoreceptor, the gene for which maps to a region of the human genome important for bone…
2007
2007
A Genome‐Wide Study of Lupus
Abstract:  Systemic lupus erythematosus (SLE) is a complex autoimmune disease in which genetics is one of the underlying risk… 
2004
2004
Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy‐like phenotype
The Albright hereditary osteodystrophy‐like (AHO‐like) syndrome was recently defined as a rare dysmorphic syndrome including… 
2002
2002
Mutations in COL 6 A 3 Cause Severe and Mild Phenotypes of Ullrich Congenital Muscular Dystrophy
INSERM U 523, Institut de Myologie, Groupe Hospitalier Pitié-Salpêtrière, Paris; Istituto di Citomorfologia Normale e Patologica… 
2001
2001
STK25 is a candidate gene for pseudopseudohypoparathyroidism.
We determined the chromosomal location of the mouse gene Stk25, encoding a member of the Ste20/PAK family of serine/threonine… 
1997
1997
RDCI, the vasoactive intestinal peptide receptor: a candidate gene for the features of Albright hereditary osteodystrophy associated with deletion of 2q37.
Albright hereditary osteodystrophy (AHO) is an autosomal dominant disorder characterised by the presence of brachymetaphalangism… 
1997
1997
Mapping NIDDM Susceptibility Loci in French Families: Studies With Markers in the Region of NIDDM1 on Chromosome 2q
Hanis et al. (1) have recently reported the mapping of a major susceptibility locus for NIDDM to human chromosome 2q37 in Mexican… 
1993
1993
The HOX complex neighbored by the EVX gene, as well as two other homeobox‐containing genes, the GBX‐class and the EN‐class, are located on the same chromosomes 2 and 7 in humans
1991
1991
A variant (2;13) translocation in rhabdomyosarcoma.
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)