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19q12

A chromosome band present on 19q
National Institutes of Health

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5 relations
19qC19orf2 wt AlleleCCNE1 wt AlleleChromosomes

Papers overview

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2006
2006
Proximal 19q Trisomy: A New Syndrome of Morbid Obesity and Mental Retardation
Aims: To report on the clinical and metabolic characteristic and the unique chromosomal defect of a mentally retarded and… 
2004
2004
Exclusion of 14 candidate loci for primary open angle glaucoma in Finnish families.
PURPOSE The aim of the present study was to examine the genetic background of primary open angle glaucoma (POAG) in the Finnish… 
2001
2001
CADASIL: Neuropsychological findings in three generations of an affected family
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary brain… 
2000
2000
Genomic alterations in primary gastric cancers analyzed by comparative genomic hybridization and clinicopathological factors.
BACKGROUND/AIMS Genetic changes during the oncogenesis and progression of gastric cancer remain unclear. The aim of our study was… 
1999
1999
No Evidence of a Major Locus for Benign Familial Infantile Convulsions on Chromosome 19q12‐q13.1
Summary: Purpose: A locus for benign familial convulsions (BFICs) has been recently mapped on chromosome 19q12–13.1 by studying… 
1998
1998
Molecular cloning of a gene on chromosome 19q12 coding for a novel intracellular protein: analysis of expression in human and mouse tissues and in human tumor cells, particularly Reed-Sternberg cells…
A novel protein, named NNX3, was molecularly characterized by cloning its cDNA, and its gene was mapped to chromosome 19q12. The… 
1992
1992
Chronic myopathy in a patient suspected of carrying two malignant hyperthermia susceptibility (MHS) mutations
Highly Cited
1989
Highly Cited
1989
Molecular cloning of human myelin‐associated glycoprotein
The nucleotide sequence for human myelin‐associated glycoprotein (MAG) and its deduced amino acid sequence, obtained by analysis… 
1989
1989
A chromosome 19 clone from a translocation breakpoint shows close linkage and linkage disequilibrium with myotonic dystrophy.
1988
1988
Localization of a human Na+,K+-ATPase alpha subunit gene to chromosome 19q12----q13.2 and linkage to the myotonic dystrophy locus.
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