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12q23

A chromosome band present on 12q
National Institutes of Health

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12qChromosomesELK3 wt Allele

Papers overview

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2019
2019
Enfermedad de Darier, variante inusual comedoniana. Presentación de un caso
Darier's disease is a rare autosomal dominant genodermatosis caused by the mutation of the ATP2A2 gene located on chromosome… 
2011
2011
[Mapping genes of major recurrent depression in genetic isolates].
We conducted a genome-wide linkage scan in two extended pedigrees ascertained from two Dagestan genetic isolates (N(o)6007 and… 
2007
2007
Investigation of novel candidate gene for inflammatory bowel disease at 12q23
2005
2005
Integration of SV 40 at 12 q 23 in SV 40-immortalized human bronchial epithelial cells
In four SV40-immortaIized human bronchial epithelial cell lines established in our laboratory, we identified the SV40 integration… 
2004
2004
Isolation and Linkage Mapping of Coding Sequences from Chicken Cosmids by Exon Trapping
We performed exon trapping in order to locate functional genes on chicken chromosomes (GGA) and to identify functional gene… 
2004
2004
Genomic Imbalances in Ependymoma by Degenerate Oligonucleotide Primed PCR-Comparative Genomic Hybridization
Background : The most consistent chromosomal abnormality in ependymomas, is loss of 22q (17-75%) and gain of 1q (0-50%). However… 
2000
2000
JUVENILE, AUTOSOMAL DOMINANT, DISTAL SPINAL MUSCULAR ATROPHY AND NEUROSENSORIAL DEAFNESS NOT LINKED TO CHROMOSOME 12q24
Distal spinal muscular atrophy, also classified as a spinal form of Charcot-Marie-Tooth-disease, or distal hereditary motor… 
1994
1994
Location of the spinal cerebellar ataxia 2 locus to a 1 cM interval on chromsome 12q23-24.1
Spinocerebellar ataxia 2 (SCA2) is a dominantly inherited neurodegenerative disorder characterised by progressive ataxia… 
1991
1991
NEUROBLASTOMA IN A CHILD WITH DUP 12Q23-]QTER DUE TO MATERNAL TRANSLOCATION WITH BREAKPOINTS ON 11Q23 AND 12Q23