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20q13

A chromosome band present on 20q
National Institutes of Health

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4 relations
20qBMP7 wt AlleleChromosomesNELFCD wt Allele

Papers overview

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2015
2015
Linear mixed models for estimating heritability and testing genetic association in family data
2009
2009
The eukaryotic translation elongation factor eEF1A2 induces neoplastic properties and mediates tumorigenic effects of ZNF217 in precursor cells of human ovarian carcinomas
  • Y. Sun
  • 2009
  • Corpus ID: 261250837
The eukaryotic translation elongation factor eEF1A2 induces neoplastic properties and mediates tumorigenic effects of ZNF217 in… 
Review
2008
Review
2008
Benigne familiäre Anfälle des Neugeborenen- und Säuglingsalters
The group of infantile and neonatal seizures belongs to the idiopathic focal epilepsies. It comprises of benign familial neonatal… 
Review
2005
Review
2005
Molecular alterations in familial colorectal cancer
............................................................................................................ 9 REVIEW OF THE… 
Review
2003
Review
2003
Genome-wide characterization of genetic aberrations in pancreatic cancer
12 INTRODUCTION 14 REVIEW OF THE LITERATURE 16 1. Pathology of pancreatic cancer 16 2. Epidemiology of pancreatic cancer 18 3… 
2002
2002
Detection of copy number changes of 20q13. 2 in transitional cell carcinomas of the urinary bladder–Tissue microarray analysis
Summary. Gains and amplifications in 20q have been reported in a number of malignancies including bladder cancer by comparative… 
1997
1997
Neue Aspekte zum Hypoparathyreoidismus und Pseudohypoparathyreoidismus im Kindes- und Jugendalter
ZusammenfassungDer Hypoparathyreoidismus (HP) ist auf eine verminderte Parathormon (PTH)-Sekretion, der… 
1996
1996
Isolated autosomal dominant typeB brachydactyly: exclusion oflinkage tocandidate regions 2q37and20q13
TypeE brachydactyly isa digital malformtration whichcharacteristical ly causes an asymmnetrical shortening of one or more… 
1982
1982
[Partial monosomy 20q : a new syndrome. Regional assignment of the ADA locus on 20q132 (author's transl)].
A karyotype 46,XY,20q-(q13 leads to qter) was found in an infant with severe mental deficiency, epilepsy, and the following… 
1977
1977
Partial trisomy 20 (20q13) and partial trisomy 21 (21pter leads to 21q21.3).
A patient with a double partial trisomy 20 and 21 with mild mental retardation and multiple congenital anomalies is presented… 
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