Zobrazeno 1 - 10
of 214
pro vyhledávání: '"E, Bocian"'
Publikováno v:
The Journal of hospital infection. 125
Disinfectants and antiseptics are important weapons to reduce the number of micro-organisms and thus limit the number of infections. Different methods of antimicrobial activity testing, often not standardized, without appropriate controls and not val
Autor:
T, Liehr, G E, Utine, U, Trautmann, A, Rauch, A, Kuechler, J, Pietrzak, J, Pietracz, E, Bocian, N, Kosyakova, K, Mrasek, K, Boduroglu, A, Weise, D, Aktas
Here we report on three new patients with neocentric small supernumerary marker chromosomes (sSMC) derived from chromosome 2, 13 and 15, respectively. The sSMC(13) and sSMC(15) had inverted duplicated shapes and the sSMC(2) a ring chromosome shape. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::350cb8c3a48a0361c70c3be9cd5c0574
https://opus4.kobv.de/opus4-fau/frontdoor/index/index/docId/3114
https://opus4.kobv.de/opus4-fau/frontdoor/index/index/docId/3114
Autor:
Robert T. Standridge, John D. Matiskella, W. F. Minor, J. C. Godfrey, P F Juby, Thomas A. Montzka, B A Hall, Richard A. Partyka, Nancy M. Cladel, R B Babel, Thomas W. Hudyma, George M. Luke, Lee C Cheney, G. E. Bocian
Publikováno v:
Journal of medicinal chemistry. 10(3)
Autor:
Judith H, Miles, T Nicole, Takahashi, Julie, Hong, Nicole, Munden, Nancy, Flournoy, Stephen R, Braddock, Rick A, Martin, Maureen E, Bocian, M Anne, Spence, Richard E, Hillman, Janet E, Farmer
Publikováno v:
American journal of medical genetics. Part A. (9)
Autism spectrum disorders (ASD) comprise a class of neurodevelopmental disorders that can originate from a variety of genetic and environmental causes. To delineate autism's heterogeneity we have looked for biologically-based phenotypes found in cons
Autor:
E, Bocian
Publikováno v:
Medycyna wieku rozwojowego. 5(3)
In the past decade, telomeres have been reported to be involved in several important biological functions. It has made the study of these chromosome regions relevant to many areas of medical and biological sciences. (Variety of basic biological funct
Publikováno v:
Ginekologia polska. 72(6)
The risk of aneuploidy in a fetus is the main reason for referral in approximately 80% of prenatal studies. Recently, a new method for rapid detection of the most frequent aneuploidies affecting chromosomes 13, 18, 21, X and Y has been developed. Flu
Autor:
P, Stankiewicz, I, Brozek, Z, Hélias-Rodzewicz, J, Wierzba, J, Pilch, E, Bocian, A, Balcerska, A, Wozniak, I, Kardaś, J, Wirth, T, Mazurczak, J, Limon
Publikováno v:
American journal of medical genetics. 101(3)
We report the results of detailed clinical and molecular-cytogenetic studies in seven patients with ring chromosome 18. Classical cytogenetics and fluorescence in situ hybridization (FISH) analysis with the chromosome 18 painting probe identified fiv
Publikováno v:
Cytogenetics and cell genetics. 83(1-2)
Publikováno v:
Pediatria polska. 71(3)
The case of a 1.5 year old girl with clinical traits of craniofacial dysmorphy, hypotonia, polydactyly and moderate mental retardation is presented. Routine cytogenetic study revealed the presence of a large additional chromosomal fragment associated
Publikováno v:
Pediatria polska. 71(3)
A reciprocal constitutive 11;22 translocation is the most frequent, non Robertsonian translocation in man. We describe a case of partial trisomy 11q and 22q in a child with facial dysmorphy, hypotonia, heart failure, cryptorchism and psychomotor reta