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18q21.32

Part of the chromosome bands present on the long (q) arm of chromosome 18.
National Institutes of Health

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4 relations
ChromosomesPHLPP1 wt AllelePMAIP1 wt Allelechromosome 18q

Papers overview

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2018
2018
Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya Syndrome
Moyamoya angiopathy (MA) is a cerebrovascular disease determining a progressive stenosis of the terminal part of the internal… 
2017
2017
Collagen and Calcium Binding EGF Domains 1 (CCBE1) in cancer – a new role past lymphatics?
Genes that influence cancer behavior continue to be the focus of a plethora of research studies, with the hopes of either… 
2015
2015
Hennekam lymphangiectasia syndrome
Hennekam lymphangiectasia syndrome is a rare autosomal recessive condition. Onset is usually in childhood. The prevalence is… 
2013
2013
Abstract LB-23: Meta-analysis of genome-wide association studies identifies multiple loci associated with chronic lymphocytic leukemia.
Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC Despite limited discovery stages (<1,125 cases… 
2012
2012
Partial monosomy 9p (9p22.2-->pter) and partial trisomy 18q (18q21.32-->qter) in a female infant with anorectal malformations.
We report a female infant with a karyotype of 46,XX,der(9)t(9;18)(p22.2;q21.32)pat and the phenotypic features of craniofacial… 
2009
2009
Characterization of a de novo balanced translocation in a patient with moderate mental retardation and dysmorphic features.
2008
2008
Sub-megabase resolution tiling (SMRT) array-based comparative genomic hybridization profiling reveals novel gains and losses of chromosomal regions in Hodgkin Lymphoma and Anaplastic Large Cell…
BackgroundHodgkin lymphoma (HL) and Anaplastic Large Cell Lymphoma (ALCL), are forms of malignant lymphoma defined by unique… 
2008
2008
Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case report
We report on a 7 years and 4 months old Greek boy with mild microcephaly and dysmorphic facial features. He was a sociable child… 
2005
2005
The paralysé (par) mouse neurological mutation maps to a 9 Mbp (4 cM) interval of mouse chromosome 18
The Paralyse mutation is a spontaneous neuromuscular mutation, first observed in 1980 at the Pasteur Institute, which is… 
2004
2004
GENETIC SUSCEPTIBILITY TO THE METABOLIC SYNDROME
The metabolic syndrome is a cluster of interrelated cardiovascular risk factors co-occurring in the same individual. People with… 
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