Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 233,381,471 papers from all fields of science
Search
Sign In
Create Free Account
20q13
A chromosome band present on 20q
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
4 relations
20q
BMP7 wt Allele
Chromosomes
NELFCD wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Linear mixed models for estimating heritability and testing genetic association in family data
Mitja Lääperi
2015
Corpus ID: 4827285
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…
Expand
Review
2008
Review
2008
Benigne familiäre Anfälle des Neugeborenen- und Säuglingsalters
M. Jacob
,
Y. Weber
,
H. Lerche
Zeitschrift für Epileptologie
2008
Corpus ID: 38786843
The group of infantile and neonatal seizures belongs to the idiopathic focal epilepsies. It comprises of benign familial neonatal…
Expand
Review
2005
Review
2005
Molecular alterations in familial colorectal cancer
T. Hienonen
2005
Corpus ID: 12595658
............................................................................................................ 9 REVIEW OF THE…
Expand
Review
2003
Review
2003
Genome-wide characterization of genetic aberrations in pancreatic cancer
E. Mahlamäki
2003
Corpus ID: 53334936
12 INTRODUCTION 14 REVIEW OF THE LITERATURE 16 1. Pathology of pancreatic cancer 16 2. Epidemiology of pancreatic cancer 18 3…
Expand
2002
2002
Detection of copy number changes of 20q13. 2 in transitional cell carcinomas of the urinary bladder–Tissue microarray analysis
D. Toncheva
,
B. Zaharieva
2002
Corpus ID: 85973469
Summary. Gains and amplifications in 20q have been reported in a number of malignancies including bladder cancer by comparative…
Expand
1997
1997
Neue Aspekte zum Hypoparathyreoidismus und Pseudohypoparathyreoidismus im Kindes- und Jugendalter
K. Kruse
Monatsschrift Kinderheilkunde
1997
Corpus ID: 45670776
ZusammenfassungDer Hypoparathyreoidismus (HP) ist auf eine verminderte Parathormon (PTH)-Sekretion, der…
Expand
1996
1996
Isolated autosomal dominant typeB brachydactyly: exclusion oflinkage tocandidate regions 2q37and20q13
Oude Luttikhuis
,
D. K. Williams
,
R. Trembath
1996
Corpus ID: 43276627
TypeE brachydactyly isa digital malformtration whichcharacteristical ly causes an asymmnetrical shortening of one or more…
Expand
1982
1982
[Partial monosomy 20q : a new syndrome. Regional assignment of the ADA locus on 20q132 (author's transl)].
J. Fraisse
,
M. Berthéas
,
F. Frère
,
B. Lauras
,
M. Rolland
,
C. Brizard
La semaine des hôpitaux : organe fondé par l…
1982
Corpus ID: 20946983
A karyotype 46,XY,20q-(q13 leads to qter) was found in an infant with severe mental deficiency, epilepsy, and the following…
Expand
1977
1977
Partial trisomy 20 (20q13) and partial trisomy 21 (21pter leads to 21q21.3).
O. Sánchez
,
P. Mamunes
,
J. Yunis
Journal of Medical Genetics
1977
Corpus ID: 40077980
A patient with a double partial trisomy 20 and 21 with mild mental retardation and multiple congenital anomalies is presented…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE