Zobrazeno 1 - 10
of 36
pro vyhledávání: '"M N, Alp"'
Publikováno v:
Journal of Pediatric Genetics. :239-242
We report a case with different chromosome Y abnormalities. Case was an 11-year-old boy, who was diagnosed with short stature, referred to laboratory of human medical genetics laboratory for genetic evaluation. Chromosomal analysis of the case was ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a021f895d9e8573c0f2e78a681ae2151
https://doi.org/10.3233/pge-12038
https://doi.org/10.3233/pge-12038
Autor:
Mehmet Fidanboy, Turgay Budak, Abdullah Gedik, Ayşegül Türkyılmaz, Halit Akbas, Sevgi Kalkanli, Hilmi Isi, M N Alp, Selda Şimşek, Mahmut Balkan, Diclehan Oral
Publikováno v:
Genetics and Molecular Research. 9:1094-1103
We reviewed cytogenetic studies performed on 4216 patients who were referred to the Cytogenetics Unit at Dicle University Hospital, Diyarbair, Southeast Turkey, between 2000 and 2009. The cases were grouped according to the reason of referral for cyt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9717d1c1ad46e337b56e47304efd6b0
https://doi.org/10.4238/vol9-2gmr827
https://doi.org/10.4238/vol9-2gmr827
Publikováno v:
Clinical and experimental obstetricsgynecology. 38(4)
To investigate the indications of amniocentesis for the detection of chromosomal abnormalities among a sample of patients in Southeast Turkey.Between 2004 and 2007, 1,068 second-trimester amniocentesis tests were performed in the Medical Biology and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::df565b952ef19337fa1c4b5bcd74784c
https://pubmed.ncbi.nlm.nih.gov/22268276
https://pubmed.ncbi.nlm.nih.gov/22268276
Autor:
A, Senyiğit, A, Yaramiş, F, Gürkan, G, Kirbaş, H, Büyükbayram, H, Nazaroğlu, M N, Alp, F, Topçu
Publikováno v:
Respiration; international review of thoracic diseases. 68(2)
Pulmonary alveolar microlithiasis (PAM) is a lung disease characterized by deposits of calcium within the alveoli. Our aim was to emphasize the familial character and the clinical features of the disease, and to draw attention to the increasing numbe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::752e1814af309a04aea09c4efc229093
https://pubmed.ncbi.nlm.nih.gov/11287838
https://pubmed.ncbi.nlm.nih.gov/11287838
Autor:
Osman, Shaibu1 (AUTHOR), Lassong, Binandam Stephen2 (AUTHOR), Dasumani, Munkaila3 (AUTHOR), Boateng, Ernest Yeboah1 (AUTHOR), Onsongo, Winnie Mokeira4 (AUTHOR), Diallo, Boubacar3 (AUTHOR), Makinde, Oluwole Daniel5 (AUTHOR)
Publikováno v:
Journal of Applied Mathematics. 5/21/2024, Vol. 2024, p1-22. 22p.
Autor:
An, Na1 (AUTHOR), Yan, Xiaoyuan2 (AUTHOR), Qiu, Qiujing2 (AUTHOR), Zhang, Zeying2 (AUTHOR), Zhang, Xiyue2 (AUTHOR), Zheng, Bowen1 (AUTHOR), Zhao, Zhenjin1 (AUTHOR), Guo, Jiajie2 (AUTHOR) guojiajie@cmu.edu.cn, Liu, Yi1 (AUTHOR) liuyi@cmu.edu.cn
Publikováno v:
Journal of Nanobiotechnology. 3/27/2024, Vol. 22 Issue 1, p1-20. 20p.
Publikováno v:
Digestive diseases and sciences. 32(2)
Relapses of Crohn's disease appear to be almost random. If these attacks could be reliably predicted, it might be possible to abort them with early treatment. In order to identify laboratory and clinical parameters that would predict an acute relapse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edd8adb34d896ef1ccbb2ea80cadb00c
https://pubmed.ncbi.nlm.nih.gov/3492346
https://pubmed.ncbi.nlm.nih.gov/3492346
Autor:
Selda Şimşek, Özlem Pamukçu Baran, Hilmi Isi, Nevin Kalkanli, Halit Akbas, Mahmut Balkan, Sevgi Kalkanli, Engin Deveci, M N Alp, Mehmet Fidanboy, Turgay Budak, Ayşegül Türkyılmaz, Diclehan Oral
Publikováno v:
Web of Science
International Journal of Morphology v.31 n.2 2013
SciELO Chile
CONICYT Chile
instacron:CONICYT
International Journal of Morphology v.31 n.2 2013
SciELO Chile
CONICYT Chile
instacron:CONICYT
El sindrome de Down es causado principalmente por la trisomia del cromosoma 21. Se revisaron los estudios citogeneticos realizados en 1.048 pacientes que fueron remitidos a la Unidad de Citogenetica del Dicle University Hospital, Diyarbakir, sudeste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e575648a7dcb0a5388dc5d83e6f879e
https://publons.com/wos-op/publon/35361462/
https://publons.com/wos-op/publon/35361462/
Autor:
Kalkanli, S.1 sgkalkanli@yahoo.com, Simsek, S.1 kalkanli@dicle.edu.tr, Balkan, M.1, Akbas, H.1, Isi, H.1, Oral, D.1, Turkyilmaz, A.1, Fidanboy, M.1, Deveci, E.2, Baran, O.2, Kalkanli, N.3, Alp, M. N.1, Budak, T.1
Publikováno v:
International Journal of Morphology. 2013, Vol. 31 Issue 2, p668-671. 4p.