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2q37

A chromosome band present on 2q
National Institutes of Health

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7 relations
ALPP wt AlleleChromosomesUGT1A LocusUGT1A1 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Biliary tract: GPC1 genetic risk further links Hedgehog signalling with pathogenesis of biliary atresia
  • Katherine Smith
  • Nature Reviews Gastroenterology &Hepatology
  • 2013
  • Corpus ID: 8259506
“Biliary atresia is the most common identifiable cause of neonatal cholestasis and is the leading cause of liver transplantation… 
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…
2008
2008
Translocation (2;11)(q37;q23) in therapy-related myelodysplastic syndrome after treatment for acute promyelocytic leukemia.
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… 
2002
2002
Novel missense mutation of the UGT1A1 gene in Thai siblings with Gilbert's syndrome
Background : Gilbert's syndrome is a common inherited disorder of bilirubin metabolism contributing to the development of… 
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… 
Review
1995
Review
1995
Clinical phenotype associated with terminal 2q37 deletion
Three children with deletions of the terminal portion of the long arm of chomosome 2 [del (2) (q37)] are described and their… 
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
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