Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 227,741,293 papers from all fields of science
Search
Sign In
Create Free Account
20p11
A chromosome band present on 20p
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
4 relations
Chromosome 20 Short Arm
Chromosomes
FLRT3 wt Allele
FOXA2 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
A Newborn with Panhypopituitarism and Seizures
Trupti Kale
,
Rachit S. Patil
,
R. Pandit
Case Reports in Genetics
2017
Corpus ID: 16061136
Interstitial deletions on the short arm of chromosome 20 are uncommon, and therefore the clinical phenotype is poorly defined…
Expand
2009
2009
Bivariate whole-genome linkage scan for bone geometry and total body fat mass.
S. Lei
,
F. Deng
,
+4 authors
Hongwen Deng
Journal of genetics and genomics = Yi chuan xue…
2009
Corpus ID: 22432914
2009
2009
Finding bald spots on chromosome 20p11
C. Doty
Clinical Genetics
2009
Corpus ID: 28398409
A genome‐wide association scan identifies new susceptibility variants for male pattern baldness on chromosome 20p11 Hillmer et al…
Expand
2007
2007
A genome-wide linkage scan for quantitative trait loci underlying obesity related phenotypes in 434 Caucasian families
Lan-Juan Zhao
,
P. Xiao
,
+4 authors
H. Deng
Human Genetics
2007
Corpus ID: 8413487
To identify quantitative trait loci (QTLs) that contribute to obesity, we performed a large-scale whole genome linkage scan (WGS…
Expand
2000
2000
Comparative genomic hybridization reveals recurrent enhancements on chromosome 20 and in one case combined amplification sites on 15q24q26 and 20p11p12 in glioblastomas.
C. Brunner
,
Volker Jung
,
Wolfram Henn
,
K. D. Zang
,
S. Urbschat
Cancer Genetics and Cytogenetics
2000
Corpus ID: 30188514
2000
2000
Fdp, a New Fibrocyte-derived Protein Related toMIA/CD-RAP, Has an in VitroEffect on the Early Differentiation of the Inner Ear Mesenchyme*
M. Cohen-Salmon
,
D. Frenz
,
W. Liu
,
E. Verpy
,
Stéphanie Voegeling
,
C. Petit
Journal of Biological Chemistry
2000
Corpus ID: 42133724
During the course of a study aimed at isolating transcripts specifically or preferentially expressed in the inner ear, we…
Expand
2000
2000
Genetic Variation in the Hepatocyte Nuclear F a c t o r-3 Gene (H N F 3 B) Does Not Contribute to Maturity-Onset Diabetes of the Young in French C a u c a s i a n s
A. Abderrahmani
,
J. Chévre
,
+7 authors
P. Froguel
2000
Corpus ID: 85655943
Mutations in genes encoding hepatocyte nuclear factor (HNF) are responsible for three of the five subtypes of maturity-onset…
Expand
1996
1996
Alagille syndrome in a family with duplication 20p11
U. Moog
,
J. Engelen
,
J. Albrechts
,
T. Hoorntje
,
F. Hendrikse
,
C. Schrander‐Stumpel
Clinical Dysmorphology
1996
Corpus ID: 22133769
Alagille Syndrome (arteriohepatic dysplasia, AHD) is a well defined genetic disorder with five major features distinctive facies…
Expand
1986
1986
Segregation analysis of rare autosomal fragile sites
S. Sherman
,
G. Sutherland
Human Genetics
1986
Corpus ID: 1037469
SummarySegregation analyses were performed on pedigrees with rare autosomal fragile sites. The results of the analysis of…
Expand
1984
1984
[Autosomal fragile sites].
M. Jotterand-Bellomo
Journal de genetique humaine
1984
Corpus ID: 43673914
It is possible to distribute the 17 autosomic fragile sites presently known in three categories according to their sensitivity…
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
or Only Accept Required