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Full Name
Düzcan, Füsun
Main Affiliation
Email
NULL
Leaving Date
01-02-2016
Source ID
738
Starting Date
30-01-1996
Country
Turkey
Status
Former staff
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Results 1-10 of 10 (Search time: 0.009 seconds).
Issue Date | Title | Author(s) | |
---|---|---|---|
1 | 2008 | A case with bloom syndrome | Kaçar, Nida ; Erdogan, Murat Kadri; Erdogan, Berna Şanlı; Atmaca, Münevver; Düzcan, Füsun |
2 | 2006 | A case with proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H) associated with urogenital anomalies | Ergin, Hacer ; Semerci, Cavidan Nur; Bican, M.; Düzcan, Füsun ; Yagci, A.B. ; Erdogan, K.M.; Tufan, Ahmet Çevik |
3 | 2003 | Cytogenetic studies in patients with reproductive failure | Düzcan, Füsun ; Atmaca, Münevver; Çetin, Gökhan Ozan ; Bağcı, Hüseyin |
4 | 2011 | Determination of apoptosis, proliferation status and O6-methylguanine DNA methyltransferase methylation profiles in different immunophenotypic profiles of diffuse large B-cell lymphoma | Türk, Nilay Şen ; Özsan, N.; Caner, Vildan ; Karagenç, Nedim ; Düzcan, F. ; Düzcan, E. ; Hekimgil, M. |
5 | 2014 | Expanding the phenotypic spectrum of ECEL1-related congenital contracture syndromes | Shaaban, S.; Düzcan, Füsun ; Yildirim, C.; Chan, W.-M.; Andrews, C.; Akarsu, N.A.; Engle, E.C. |
6 | 2012 | Expression of ERCC1 and its clinicopathological correlations in non-small cell lung cancer | Tepeli, Emre ; Caner, Vildan ; Büyükpınarbaşılı, N.; Çetin, Gökhan Ozan ; Düzcan, Füsun ; Elmas, Levent ; Bağcı, Gülseren |
7 | 2003 | Familial influence on parkinsonism in a rural area of Turkey (Kizilcaboluk-Denizli): A community-based case-control study | Düzcan, Füsun ; Zencir, Mehmet ; Özdemir, Fatma; Çetin, Gökhan Ozan ; Bağcı, Hüseyin ; Heutink, P.; Bonifati, V. |
8 | 2008 | No strong association between HER-2/neu protein overexpression and gene amplification in high-grade invasive urothelial carcinomas | Caner, Vildan ; Türk, Nilay Şen ; Düzcan, Füsun ; Tufan, N.L.S.; Kelten, Esra Canan; Zencir, S.; Dodurga, Yavuz |
9 | 2012 | Patient with 45,X karyotype and severe virilization occult y sequences | Çorduk, Nergül; Semiz, Serap ; Koltuksuz, Uğur ; Semerci, C.Nur; Düzcan, Füsun ; Düzcan, Ender; Şatıroğlu-Tufan, Naciye Lale |
10 | 2009 | Pseudohypoparathyroidism type IA (PHP-Ia): Maternally inherited GNAS gene mutation | Semiz, Serap ; Düzcan, Füsun ; Candemir, M.; Caner, Vildan ; Thiele, S.; Semiz, E.; Hiort, O. |