Unbound MEDLINE

Chromosomes, Human, Pair 16 journal articles from PubMed MEDLINE database

Unbound MEDLINE results for:Bookmark this site
Chromosomes, Human, Pair 16[MH]| Refine this search
1 - 10 of 2898 journal articles in the PubMed databaseEmail to a friend    
 
Kim J, Park TS, Song J, et al. 
Detection of FUS-ERG chimeric transcript in two cases of acute myeloid leukemia with t(16;21)(p11.2;q22) with unusual characteristics. [Journal Article]
Cancer Genet Cytogenet 2009 Oct 15; 194(2):111-8.
Abstract | Full Citation | Publisher Full Text | Find Related Articles 
Belzil VV, Valdmanis PN, Dion PA, et al. 
Mutations in FUS cause FALS and SALS in French and French Canadian populations. [JOURNAL ARTICLE]
Neurology 2009 Sep 9.
Abstract | Full Citation | Publisher Full Text | Find Related Articles 
Ticozzi N, Silani V, Leclerc AL, et al. 
Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort. [JOURNAL ARTICLE]
Neurology 2009 Sep 9.
Abstract | Full Citation | Publisher Full Text | Find Related Articles 
Cavazzini F, Bardi A, Ciccone M, et al. 
Trisomy 8 in PDGFRB-negative cells in a patient with imatinib-sensitive chronic myelomonocytic leukemia and t(5;16)(q33;p13), PDGFRB-NDE1 fusion. [Letter, Research Support, Non-U.S. Gov't]
Cancer Genet Cytogenet 2009 Oct; 194(1):67-9.
Full Citation | Publisher Full Text | Find Related Articles 
Melo JB, Matoso E, Polityko A, et al. 
Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation. [Journal Article]
Cytogenet Genome Res 2009; 125(2):109-14.
Abstract | Full Citation | Publisher Full Text | Find Related Articles 
Prébet T, Boissel N, Reutenauer S, et al. 
Acute myeloid leukemia with translocation (8;21) or inversion (16) in elderly patients treated with conventional chemotherapy: a collaborative study of the French CBF-AML intergroup. [Journal Article]
J Clin Oncol 2009 Oct 1; 27(28):4747-53.
Abstract | Full Citation | Publisher Full Text | Find Related Articles 
Kuroda N, Michal M, Hes O, et al. 
Renal angiomyoadenomatous tumor: fluorescence in situ hybridization. [Letter]
Pathol Int 2009 Sep; 59(9):689-91.
Full Citation | Publisher Full Text | Find Related Articles 
Chen YY, Hwang ES, Roy R, et al. 
Genetic and Phenotypic Characteristics of Pleomorphic Lobular Carcinoma In Situ of the Breast. [JOURNAL ARTICLE]
Am J Surg Pathol 2009 Aug 20.
Abstract | Full Citation | Publisher Full Text
Vorsanova SG, Voinova VI, Iurov II, et al. 
[Cytogenetic, molecular cytogenetic, clinical and genealogical study of mothers of children with autism: a search for family genetic markers of autistic disorders.] [JOURNAL ARTICLE]
Zh Nevrol Psikhiatr Im S S Korsakova 2009; 109(6):54-64.
Abstract | Full Citation
Lipton J, Rivkin MJ 
16p11.2-related paroxysmal kinesigenic dyskinesia and dopa-responsive parkinsonism in a child. [Case Reports, Journal Article]
Neurology 2009 Aug 11; 73(6):479-80.
Full Citation | Publisher Full Text | Find Related Articles 
New Search Next Results
  

Enter
www.unboundmedicine.com/medline
in your iPhone browser
or View our
Unbound MEDLINE
iPhone demo


Advertise on this site.