Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Şehime Gülsüm Temel"'
Autor:
Pinar Tulay, Mahmut Cerkez Ergoren, Ahmet Alkaya, Eyup Yayci, Sebnem Ozemri Sag, Sehime Gulsum Temel
Publikováno v:
Global Medical Genetics, Vol 07, Iss 04, Pp 128-132 (2020)
Purpose Turner syndrome is a sex chromosomal aberration where majority of the patients have 45,X karyotype, while several patients are mosaic involving 45,X/46,XX; 46,X,i(Xq); and other variants. Cytogenetic analysis, karyotyping, is considered to be
Externí odkaz:
https://doaj.org/article/7aa8ab43a85d400bbb18cdb8f0e42318
Autor:
Emel Bülbül Başkan, Asli Gorek Dilektasli, Esra Uzaslan, Şehime Gülsüm Temel, Dilara Omer, Şebnem Özemri Sağ
Publikováno v:
Turkiye Klinikleri Archives of Lung. 20:62-67
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7e135ae8b004ef5697bc143cac1463f
https://doi.org/10.5336/archlung.2020-79774
https://doi.org/10.5336/archlung.2020-79774
Autor:
Ayhan Kubar, Sehime Gülsüm Temel, Serdar Beken, Gizem Onder, Ozden Hatirnaz, Ayse Korkmaz, Yasemin Alanay, Ugur Ozbek, Sebnem Ozemri Sag, Mahmut Cerkez Ergoren, Elif Kubar, Candan Zeynep Sonmezalp, Ozlem Doğan
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 12, Pp n/a-n/a (2023)
Abstract Background Nucleic acid‐based assays provide an opportunity to screen for genetically encoded diseases like spinal muscular atrophy (SMA), before the onset of symptoms. Nowadays, such assays could be easily utilized as high‐throughputs i
Externí odkaz:
https://doaj.org/article/8e9b296ac0c9461bbb8e809e7092feb7