Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ceyhan Sayar"'
Publikováno v:
Results in Engineering, Vol 20, Iss , Pp 101421- (2023)
Next-generation sequencing (NGS) technologies have completely changed the field of genomics by making it possible to rapidly and inexpensively produce genome-scale sequence data with higher precision and resolution. In recent years, rapid technologic
Externí odkaz:
https://doaj.org/article/25b8311dcccb4781b09764faf5b962ce
Publikováno v:
Gazi Medical Journal. 29
Complex chromosome rearrangements (CCR’s) involving multiple breaks in two or more chromosomes are rare. The precise characterization of a CCR is difficult and may be inaccurate even by using molecular cytogenetic techniques. Various new molecular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a806bf3176b8ec254f4726d7d3caee3
https://doi.org/10.12996/gmj.2018.73
https://doi.org/10.12996/gmj.2018.73
Autor:
B Devranoglu, Soylemez, Gozde Yesil, Ali Karaman, Hatip Aydin, Ceyhan Sayar, Güven Toksoy, Bilge Geckinli
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology. 182:211-215
Our objective was to identify the distribution of cytogenetic abnormalities of 175 Turkish women with primary amenorrhea (PA) or premature ovarian insufficiency (POI). A retrospective study was performed using medical records of 94 patients with PA a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c9a3579d80616ff7f6c9914533f9ca6
https://doi.org/10.1016/j.ejogrb.2014.09.033
https://doi.org/10.1016/j.ejogrb.2014.09.033
Publikováno v:
International Journal of Gynecology & Obstetrics. 85:24-29
Objectives: In this study, the aims were to reveal the incidence of isolated choroid plexus cyst in our population, and to discuss the accuracy of distinguishing either an isolated or non-isolated choroid plexus cyst. Methods: The study population wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91f5c2d9d71235d4955fb4dc5dcdf3c3
https://doi.org/10.1016/j.ijgo.2003.08.016
https://doi.org/10.1016/j.ijgo.2003.08.016
Publikováno v:
The Turkish journal of pediatrics. 51(2)
We report a patient with severe developmental delay, failure to thrive, microbrachycephaly, large anterior fontanel, ocular hypertelorism, broad nasal bridge, low-set ears, long philtrum, micrognathia, partial cleft palate, broad distal digits, abnor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::99fea0c98597db49542a64987b6c59da
https://pubmed.ncbi.nlm.nih.gov/19480332
https://pubmed.ncbi.nlm.nih.gov/19480332
Publikováno v:
Molecular Therapy. 13
Introduction: Procalcitonin (PCT) was originally described in 1984 as a 116 aminoacid protein with a molecular weight of 14.5 kDa. The PCT gene, referred to as Calc-1, is located on chromosome 11p15.4 and was sequenced in 1989. The promoter has sites
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d99cd5b7f9bad43da068d666f9f788e7