Claim profile
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
Loading...
5
0
20
0
false
Loading...
6
0
20
0
false
Results 1-20 of 23 (Search time: 0.035 seconds).
| Issue Date | Title | Author(s) | |
|---|---|---|---|
| 1 | 2008 | Bloom sendromlu bir olgu sunumu | Kaçar, Nida ; Erdoğan, Murat Kadri; Erdoğan, Berna Şanlı; Atmaca, Münevver; Düzcan, Füsun |
| 2 | 2009 | A case of schizophrenia accompanying velocardiofacial syndrome | Şengül, Cem ; Efe, Muharrem ; Tepeli, Emre ; Çetin, Gökhan Ozan ; Düzcan, Füsun ; Herken, Hasan |
| 3 | 2008 | A case with bloom syndrome | Kaçar, Nida ; Erdogan, Murat Kadri; Erdogan, Berna Şanlı; Atmaca, Münevver; Düzcan, Füsun |
| 4 | 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 |
| 5 | 2003 | Cytogenetic studies in patients with reproductive failure | Düzcan, Füsun ; Atmaca, Münevver; Çetin, Gökhan Ozan ; Bağcı, Hüseyin |
| 6 | 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. |
| 7 | 2023 | Dicentric Recombinant Chromosome 18 due to Maternal Paracentric Inversion Analyzed by Array CGH | Anlas, Özlem; Ölmez, Akgun; Karaman, Birsen; Düzcan, Füsun ; Yüksel, Selçuk ; Tümkaya, Funda ; Bağcı, Gülseren ; Gunduz, Cavidan Nur Semerci |
| 8 | 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. |
| 9 | 2011 | Expression and amplification of topoisomerase-2? in type 1 and type 2 papillary renal cell carcinomas and its correlation with HER2/neu amplification | Düzcan, Füsun ; Duzcan, S.E.; Sen, S.; Yorukoglu, K.; Caner, Vildan ; Şen Türk, Nilay ; Çetin, Gökhan Ozan |
| 10 | 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 |
| 11 | 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. |
| 12 | 2010 | Familial translocation (2;18) ascertained through recurrent spontaneous abortions [Article] | Bağcı, Gülşen; Tepeli, Emre ; Düzcan, Füsun ; Çetin, G. Ozan ; Alataş, Erkan |
| 13 | 2003 | İki ayrı ailede perisentrik inversiyon: inv(4)(p16q12) | Bal, Filiz; Düzcan, Füsun ; Atmaca, Münevver; Balcı, Ayşe |
| 14 | 2002 | Laurence-Moon-Biedl syndrome with vaginal atresia | Kara, İnci Gökalan ; Düzcan, Füsun ; Aktan, Erdal |
| 15 | 2006 | MURCS birlikteliği ile tek taraflı over agenezisi | Yıldırım, Başak; Semerci Gündüz, Cavidan Nur ; Yağcı, Ahmet Baki ; Duman, Koray; Düzcan, Füsun |
| 16 | 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 |
| 17 | 2003 | Otozomal resesif işitme kaybı olan bir olguda aile öyküsü, klinik ve moleküler incelemeler | Düzcan, Füsun ; Wollnık, Bernd; Tepeli, Emre ; Ardıç, Fazıl Necdet ; Uyguner, Oya; Bağcı, Hüseyin |
| 18 | 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 |
| 19 | 2005 | Prenatal diagnosis of a trisomy 13 case associated with holoprosencephaly by ultrasonography and quantitative fluorescent PCR | Şatiroğlu Tufan; Tufan, Ahmet Çevik ; Yildirim, B.; Kaleli, Babür ; Semerci, C.Nur; Bir, Ferda ; Düzcan, Füsun ; Bağcı, Hüseyin |
| 20 | 2002 | Progressive autosomal dominant optic atrophy and sensorineural hearing loss in a Turkish family. | Ozden S; Düzcan, Füsun ; Wollnik B; Cetin OG; Sahiner T; Bayramoğlu I; Yüksel-Apak M |