Zobrazeno 1 - 10
of 139
pro vyhledávání: '"Lüleci, Güven"'
Germline mutations of BRCA1 and BRCA2 genes in Turkish breast, ovarian, and prostate cancer patients
Autor:
Manguoğlu, Esra, Güran, Şefik, Yamaç, Deniz, Çolak, Taner, Şimşek, Mehmet, Baykara, Mehmet, Akaydın, Mustafa, Lüleci, Güven
Publikováno v:
In Cancer Genetics and Cytogenetics 2010 203(2):230-237
Autor:
Sargın, Canan Figen *, Berker-Karaüzüm, Sibel, Manguoğlu, Esra, Erdoğru, Tibet, Karaveli, Şeyda, Gülkesen, Kemal Hakan, Baykara, Mehmet, Lüleci, Güven
Publikováno v:
In Annales de genetique 2004 47(1):61-68
Publikováno v:
In Cancer Genetics and Cytogenetics 2002 132(1):36-40
Akademický článek
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Publikováno v:
Volume: 13, Issue: 1 30-32
Marmara Medical Journal
Marmara Medical Journal
A one-year-old boy with the short arm deletion of chromosome 18 is reported. The case has IgA deficiency and facial dysmorphism. Chromosome analysis showed that his father had 32% premature centromere division (PCD). The deletion of short arm of chro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::a14efd9887f4f255ac6421d3d0641365
https://dergipark.org.tr/tr/pub/marumj/issue/25793/272030
https://dergipark.org.tr/tr/pub/marumj/issue/25793/272030
Publikováno v:
Volume: 13, Issue: 1 7-10
Marmara Medical Journal
Marmara Medical Journal
Objective: The aim of this study was to optimize the diagnosis of the fragile X syndrome in six large families with fragile X syndrome in Turkey.Methods: Southern blot analysis was performed to identify the mutations of the FMR 1 gene localized on FR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::9fe95e6cde564e84084bf873a3113d8b
https://dergipark.org.tr/tr/pub/marumj/issue/25793/272023
https://dergipark.org.tr/tr/pub/marumj/issue/25793/272023
Autor:
BAĞCI, Gülseren, ALPER, Özgül, HAGEMEİJER, Anne, ACAR, Hasan, SMİT, Elizabeth, ÜNER, Mine, LÜLECİ, Güven
Publikováno v:
Volume: 17, Issue: 2 81-83
Marmara Medical Journal
Marmara Medical Journal
İleri anne yaşı ve üçlü testte 1/14 risk ile Down sendromu düşünülen gebeliğe 19. haftasında amniyosentez uygulandı. Fetusun kromozom analizi sonucu karyotipi 46,XX,inv (17) (p11.2;q25.1) olarak belirlendi. Sitogenetik olarak tespit edil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::252a01edfc6ce69c5a4671086c11daa1
https://dergipark.org.tr/tr/pub/marumj/issue/418/3140
https://dergipark.org.tr/tr/pub/marumj/issue/418/3140
Autor:
KESER, İbrahim, MANGUOĞLU, Esra, KAYIŞLI, Özlem GÜZELOĞLU, KURT, Fatma, MENDİLCİOĞLU, İnanç, ŞİMŞEK, Mehmet, BAĞCI, Gülseren, KÜPESİZ, Alpan, LÜLECİ, Güven
Publikováno v:
Volume: 35, Issue: 4 253-255
Turkish Journal of Medical Sciences
Turkish Journal of Medical Sciences
Beta-thalassemia and Sickle cell anemia are serious health problems in the Antalya Province of Turkey as well as World Wide. We aimed to summarize data obtained from the prenatal diagnosis for beta-thalassemia and sickle cell anemia of 103 fetuses. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::bf9f36cc05853e4297e0783a1819dd6d
https://dergipark.org.tr/tr/pub/tbtkmedical/issue/12339/147885
https://dergipark.org.tr/tr/pub/tbtkmedical/issue/12339/147885
Autor:
GÜZELOĞLU KAYIŞLI, Özlem, KESER, İbrahim, CANATAN, Duran, ŞANLIOĞLU, Ahter, ÖZEŞ, Osman Nidai, LÜLECİ, Güven
Publikováno v:
Volume: 35, Issue: 3 175-177
Turkish Journal of Medical Sciences
Turkish Journal of Medical Sciences
Key Words: b-thalassemia, b-globin gene, insertion, frameshift mutation, DNA sequencing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::24883949dadeeda763344cedbc8f7f93
https://dergipark.org.tr/tr/pub/tbtkmedical/issue/12340/147897
https://dergipark.org.tr/tr/pub/tbtkmedical/issue/12340/147897
Publikováno v:
Volume: 41, Issue: 5 945-948
Turkish Journal of Medical Sciences
Turkish Journal of Medical Sciences
To report a rare chromosomal abnormality, familial satellited Y chromosome (Yqs), in 3 Turkish prenatal cases. Material and methods: Metaphase chromosomes were prepared from amniocytes for prenatal cases and from lymphocytes for their fathers accordi