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3q26.3-q27
A chromosome band present on 3q
National Institutes of Health
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2 relations
Chromosomes
LAMP3 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
High sex determining region Y-box 2 expression is a negative predictor of occult lymph node metastasis in early squamous cell carcinomas of the oral cavity
Zullig
2017
Corpus ID: 33356296
2016
2016
Gene mapping in an anophthalmic pedigree of a consanguineous Pakistani family opened new horizons for research
S. Saleha
,
M. Ajmal
,
S. Zafar
,
A. Hameed
Balkan Journal of Medical Genetics
2016
Corpus ID: 18330422
ABSTRACT Clinical anophthalmia is a rare inherited disease of the eye and phenotype refers to the absence of ocular tissue in the…
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2014
2014
SOX2 and cancer literatures
Hongbao Ma
,
M. Young.
2014
Corpus ID: 49608903
SRY (sex determining region Y)-box 2 (SOX2), is a transcription factor that is essential for maintaining self-renewal, or…
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2012
2012
A Rare Chromosome 3 Imbalance and Its Clinical Implications
K. Sims
,
R. Mazzaschi
,
Emilie Payne
,
I. Hayes
,
D. Love
,
A. George
Case Reports in Pediatrics
2012
Corpus ID: 1167953
The duplication of chromosome 3q is a rare disorder with varying chromosomal breakpoints and consequently symptoms. Even rarer is…
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2008
2008
Neocentromere marker chromosome of distal 3q mimicking dup(3q) syndrome phenotype
K. Izumi
,
Y. Yamashita
,
+4 authors
K. Kosaki
American Journal of Medical Genetics. Part A
2008
Corpus ID: 31446008
Supernumerary marker chromosomes (SMCs) lacking alpha‐satellite sequences and possessing a newly derived functional centromere…
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2006
2006
Multiple forms of genetic instability within a 2‐Mb chromosomal segment of 3q26.3–q27 are associated with development of esophageal adenocarcinoma
Lin Lin
,
Zhuwen Wang
,
+9 authors
D. Beer
Genes, Chromosomes and Cancer
2006
Corpus ID: 24808589
Gene amplification is one of the mechanisms to activate oncogenes in many cancers, including esophageal adenocarcinoma (EA). In…
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2005
2005
Novel case of dup(3q) syndrome due to a de novo interstitial duplication 3q24‐q26.31 with minimal overlap to the dup(3q) critical region
M. Meins
,
Javad Karimzad Hagh
,
+4 authors
J. Epplen
American Journal of Medical Genetics. Part A
2005
Corpus ID: 32919938
Dup(3q) syndrome is characterized by typical facial features, mental and growth retardation, often with congenital heart defects…
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1999
1999
Familial Dominant Thrombocytopenia: Clinical, Biologic, and Molecular Studies
A. Iolascon
,
S. Perrotta
,
+4 authors
A. Savoia
Pediatric Research
1999
Corpus ID: 4906482
Inherited thrombocytopenias are a heterogenous group of disorders. Different criteria have been suggested to classify the forms…
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