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Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly
(Blackwell MunksgaardFrederiksberg CDinamarca, 2005)
Atypical copy number abnormalities in 22q11.2 region: Report of three cases
(Elsevier Science BvAmsterdamHolanda, 2013)
Comparative genomic hybridization analysis detects frequent over-representation of DNA sequences at 3q, 7p, and 8q in head and neck carcinomas
(Elsevier B.V., 2000-05-01)
Comparative genomic hybridization (CGH) was used to identify chromosomal imbalances in 19 samples of squamous cell carcinoma of the head and neck (HNSCC). The chromosome arms most often or er-represented were 3q (48%), 8q ...
Radii of starlikeness and convexity of some q-Bessel functions
(2016-03-01)
Geometric properties of the Jackson and Hahn-Exton q-Bessel functions are studied. For each of them, three different normalizations are applied in such a way that the resulting functions are analytic in the unit disk of ...
In silico studies of Coxiella burnetii outer membrane proteins (OMPs) as basis to Q fever diagnosis development
(Fiocruz/Instituto de Tecnologia em Imunobiológicos, 2019)
Multiple attribute group decision‐making based on order‐α divergence and entropy measures under q‐rung orthopair fuzzy environment
(Wiley, 2020)
The q-rung orthopair fuzzy set ((ROPFS)-R-q), proposed by Yager, is a more effective and proficient tool to represent uncertain or vague information in real-life situations. Divergence and entropy are two important measures, ...
A de novo interstitial 6q deletion in a boy with a split hand malformation
(Journal of Applied Genetics 48(4), 2007, pp. 405-407, 2015)
Translocation (11;19)(q23;p13.3) associated with a novel t(5;16) (ql3;q22) in a patient with acute myelocytic leukemia
(Elsevier B.V., 2003-02-01)
A novel association of t(11;19)(q23;p13) and t(5;16)(q13;q22) was detected by G-banding and spectral karyotyping studies in an 18-year-old patient. While balanced t(11; 19) has been often described in acute myelocytic ...
Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in Autism Spectrum Disorder Brazilian Individuals with and without Epilepsy
(Magnolia PressSan Francisco, 2014-09)
Copy number variations (CNVs) are an important cause of ASD and those located at 15q11-q13, 16p11.2 and 22q13 have been reported as the most frequent. These CNVs exhibit variable clinical expressivity and those at 15q11-q13 ...