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19p13

A chromosome band present on 19p
National Institutes of Health

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6 relations
CD209 wt AlleleCDKN2D wt AlleleChromosome 19 Short ArmChromosomes

Papers overview

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2018
2018
Abstract GS3-07: Genome-wide copy number analysis of chemotherapy-resistant metastatic triple-negative breast cancer from cell-free DNA
Introduction: Triple-negative breast cancer (TNBC) is a poor prognosis breast cancer subset characterized by relatively few… 
2017
2017
Role of CDKN2C Fluorescence In Situ Hybridization in the Management of Medullary Thyroid Carcinoma
&NA; Medullary thyroid carcinoma (MTC), an aggressive form of thyroid cancer, occurs sporadically in approximately 75% of MTCs… 
2017
2017
Days 1 and 2 ) Day 1-Plenary Session # 1 Complexity of Decision-Making in Surgical Care Provided in Patient Portals
s for Presentation and Poster Plenary Sessions (Days 1 and 2) Day 1 Plenary Session #1 Complexity of Decision-Making in Surgical… 
2016
2016
Correction: Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer
Nat. Genet. 42, 880–884 (2010); published online 19 September 2010; corrected after print 7 December 2015 In the version of this… 
2011
2011
Effects of SNPs at newly identified lipids loci on blood lipid levels and risk of coronary heart disease in Chinese Han population: A case control study
Associations between “lipid-related” candidate genes, blood lipid concentrations and coronary artery disease (CHD) risk are not… 
2006
2006
Fine-mapping of the coeliac disease linkage region on chromosome 19p13 reveals a new player in the field
2000
2000
Familial Hemiplegic Migraine, A Case Report Of Attack Associated Findings
Recent studies have shed more light onto the genetical basis of familial hemiplegic migraine (FHM) as a channelopathy due to 3… 
1997
1997
Assignment of the porcine nuclear factor I/CTF (NFI/CTF) gene to Chromosome 2q12-13 by FISH
Species: Pig (Sus scrofa domestica) Locus name: Nuclear Factor I/CTF Locus symbol: NFI/CTF Map position: 2q12-13 Method of… 
1995
1995
Familial Periodic Cerebellar AtaxiawithoutMyokymiaMapstoa 19-cMRegion on 19p13
Summary Familial periodic cerebellar ataxia (FPCA) isaheterogenousgroup ofrare autosomal dominant disorders characterized… 
1994
1994
Recurrent cytogenetic aberrations and loss of constitutional heterozygosity in ovarian carcinomas.
Cancer is regarded as the result of the accumulation of multiple genetic changes leading to either the activation of oncogenes… 
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