Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Dilara SÜLEYMANOVA"'
Autor:
Nilgün TANRIVERDİ, Ayfer PAZARBAŞI, Dilara Süleymanova KARAHAN, İlker GÜNEY, Deniz TAŞTEMİR, Erdal TUNÇ, Osman DEMİRHAN, Özlem HERGÜNER
Publikováno v:
Cukurova Medical Journal, Vol 38, Iss 3, Pp 540-545 (2013)
Giriş: Zeka geriliği, genel populasyonda %2-3 gibi oldukça yüksek bir oranda bulunan ve vakaların %50"sinden fazlasında sebebi bulunamayan bir sağlık problemidir. En önemli nedenlerinden birisi kromozom düzensizlikleri olup hasta seçimi ve
Externí odkaz:
https://doaj.org/article/e82f085f51e243bc8969ec56328fc47b
Autor:
Dilara SÜLEYMANOVA, Kübra TEMOÇiN
Publikováno v:
European Journal of Therapeutics. 6:116-120
Two patients who applied to our Genetics Unit with multiple congenital anomalies were examined for pedigree and cytogenetical analyses. The patients were diagnosed as Multiple Pterygium Syndrome(MPS) and medical genetic counselling was given to the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ff29e929f8811155f28df634dd2eeff
https://doi.org/10.58600/eurjther.1995-6-1-1568-arch
https://doi.org/10.58600/eurjther.1995-6-1-1568-arch
Autor:
Dilara SÜLEYMANOVA, A.Kübra TEMOÇİN, Bilgin YÜKSEL, Mustafa YILMAZ, Mustafa GÖĞEBAKAN, Meltem PIRTI, Mehdi TASAUJİ
Publikováno v:
European Journal of Therapeutics. 6:121-124
Genetic consultation was given to three children with microcephaly, mental retardation, and spastic diplegia.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::279c52ca8aa6e6d7eaf39f92ec449167
https://doi.org/10.58600/eurjther.1995-6-1-1569-arch
https://doi.org/10.58600/eurjther.1995-6-1-1569-arch
Publikováno v:
Global Journal of Fertility and Research. 1:006-010
Aim of the study: Infertility is a relatively common health condition, affecting nearly 15% of all couples, and has been estimated that nearly 50% of infertility cases are due to genetic defects.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fda48d2750e015c2e688adf144ac96c6
https://doi.org/10.17352/gjfr.000002
https://doi.org/10.17352/gjfr.000002
Publikováno v:
Volume: 47, Issue: 5 1447-1455
Turkish Journal of Medical Sciences
Turkish Journal of Medical Sciences
Background/aim: The genetic background of Turner syndrome (TS) is highly variable. The correlation between genotype and phenotype is not yet well understood. The aim of this study was to describe the frequencies and distributions of Turner karyotypes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::1f7590fcdf7f4ccda8d89b487e9df9b9
https://dergipark.org.tr/tr/pub/tbtkmedical/issue/45689/576372
https://dergipark.org.tr/tr/pub/tbtkmedical/issue/45689/576372
Today, breast cancer (BC) is the most commonly occurring cancer among women. Several studies have suggested that the proportion of BC can be attributed to a genetic factor that may be as high as 30%. The aim of the present study was to describe the t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e2fad61dd7de9b95f54f7185145d384
PubMedID: 26874988 In this retrospective study, karyotype results of 1510 couples with a history of recurrent spontaneous abortion were evaluated. The study was conducted at BalcalI Hospital in Adana region of Turkey. For all cases, peripheral blood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1231bb62da57308489063788d23ef50
https://hdl.handle.net/20.500.12605/11962
https://hdl.handle.net/20.500.12605/11962
Autor:
Erdal Tunç, Dilara Süleymanova-Karahan, Derya Gümürdülü, Osman Demirhan, Deniz Taştemir, Ayfer Pazarbaşı
Publikováno v:
Balkan Journal of Medical Genetics, Vol 11, Iss 1, Pp 69-74 (2008)
Prenatal Diagnosis of Translocation 13;13 Patau Syndrome: Clinical Features of Two CasesPatau syndrome is associated with extra chromosome 13 material, either free as in the 47,++13 or in a Robertsonian translocation or another rearrangement. We repo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69d3ca82b64d630e77a8d79c1370ee7b
https://doi.org/10.2478/v10034-008-0021-1
https://doi.org/10.2478/v10034-008-0021-1
Publikováno v:
Human Genetics & Embryology.
Objectives: Hypogonadism is the clinical manifestation of the impaired function of the testes and the ovaries, and is either due to endocrinological problems or chromosomal abnornlalities (CA). Chromosomal analysis is one important piece in the hypog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0a453456f28ac7c0433487eba07c476
https://doi.org/10.4172/2161-0436.1000124
https://doi.org/10.4172/2161-0436.1000124
Autor:
TANRIVERDİ, Nilgün, PAZARBAŞI, Ayfer, KARAHAN, Dilara Süleymanova, GÜNEY, İlker, TAŞTEMİR, Deniz, TUNÇ, Erdal, DEMİRHAN, Osman, HERGÜNER, Özlem
Publikováno v:
Volume: 38, Issue: 3 540-545
Cukurova Medical Journal
Cukurova Medical Journal
Purpose: Mental retardation is a common handicap (2-3% of the general population) with an unknown cause in more than 50% of mentally retarded patients. Important causes are chromosome abnormalities which are detectable in 4-28% of cases, depending on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::45ff818bc299663e46d4c25df4d1827d
https://dergipark.org.tr/tr/pub/cumj/issue/4194/55293
https://dergipark.org.tr/tr/pub/cumj/issue/4194/55293