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of 82
pro vyhledávání: '"YİRMİBEŞ KARAOĞUZ, MERAL"'
Autor:
Tuğ, Esra, Yirmibeş Karaoğuz, Meral, Kazan, Hasan Hüseyin, Ergün, Mehmet Ali, Kazancıoğlu, Elvin
Background: Small non-coding micro ribonucleic acids,namely miRNAs or MIRs are associated with defective placentation due to theirrole on the proliferation of the trophoblasts. Relationship between theabortion development and placental defects lead u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10046::10ed0872260fb544e44a4feaf745849a
https://avesis.gazi.edu.tr/publication/details/20a6d6c5-2f90-4976-8ef7-c2941cabc3f3/oai
https://avesis.gazi.edu.tr/publication/details/20a6d6c5-2f90-4976-8ef7-c2941cabc3f3/oai
Duplication of the short arm (p) of chromosome (Chr.) 9 is a frequently seen abnormality while duplication of both p and long arm (q) is a rare chromosomal rearrangement derived mostly from parental translocations or inversions. The unbalanced produc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10046::52e1068c82b43dd606624cc95decc2b5
https://avesis.gazi.edu.tr/publication/details/8c26cf97-5424-404e-97a3-f617e74ba6df/oai
https://avesis.gazi.edu.tr/publication/details/8c26cf97-5424-404e-97a3-f617e74ba6df/oai
Publikováno v:
Volume: 85, Issue: 2 279-284
Journal of Istanbul Faculty of Medicine
Journal of Istanbul Faculty of Medicine
Duplication of the short arm (p) of chromosome (Chr.) 9 is a frequently seen abnormality while duplication of both p and long arm (q) is a rare chromosomal rearrangement derived mostly from parental translocations or inversions. The unbalanced produc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::51ae3e0efcce5c6c4349cd8aa8e16ab5
https://dergipark.org.tr/tr/pub/iuitfd/issue/68433/1038997
https://dergipark.org.tr/tr/pub/iuitfd/issue/68433/1038997
Autor:
BAKIR, Abdullatif1, YİRMİBEŞ KARAOĞUZ, Meral2, PERÇİN, Ferda Emriye2, TUĞ, Esra2 esratug@hotmail.com, CİNAZ, Peyami3, ERGÜN, Mehmet Ali2
Publikováno v:
Turkish Journal of Medical Sciences. 2018, Vol. 48 Issue 2, p386-390. 5p.
Akademický článek
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Objective: Clinical application of sequence comparative genomic hybridization has greatly contributed to the diagnosis of patients with multiple congenital anomalies, syndromic or non-syndromic intellectual disability. The idiopathic intellectual dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2a5b804fa86f3ed957940e895456e44
https://avesis.gazi.edu.tr/publication/details/8f3f40a8-5556-44b2-90fe-71d9e922c6d3/oai
https://avesis.gazi.edu.tr/publication/details/8f3f40a8-5556-44b2-90fe-71d9e922c6d3/oai
Autor:
ÇETİN, EBRU, CİCİOĞLU, HALİL İBRAHİM, YİRMİBEŞ KARAOĞUZ, MERAL, KURTULUŞ, MELAHAT, ALP, EBRU, Kesici, Tahsin, ÇELENK, ÇAĞRI, GÜNAY, MEHMET
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10046::457cac5fca1558f2309be846fd78db79
https://avesis.gazi.edu.tr/publication/details/bc990c21-a333-40e8-8ca9-e0219a3b323f/oai
https://avesis.gazi.edu.tr/publication/details/bc990c21-a333-40e8-8ca9-e0219a3b323f/oai