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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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6
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Subject
- 11 article
- 11 human
- 8 female
- 7 male
- 6 case report
- 6 Humans
- 5 Female
- 5 Male
- 4 controlled study
- 3 adolescent
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Type
- 16 Article
Fulltext
Results 1-16 of 16 (Search time: 0.009 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 | 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. |
7 | 2003 | İki ayrı ailede perisentrik inversiyon: inv(4)(p16q12) | Bal, Filiz; Düzcan, Füsun ; Atmaca, Münevver; Balcı, Ayşe |
8 | 2002 | Laurence-Moon-Biedl syndrome with vaginal atresia | Kara, İnci Gökalan ; Düzcan, Füsun ; Aktan, Erdal |
9 | 2006 | MURCS birlikteliği ile tek taraflı over agenezisi | Yıldırım, Başak; Semerci Gündüz, Cavidan Nur ; Yağcı, Ahmet Baki ; Duman, Koray; Düzcan, Füsun |
10 | 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 |
11 | 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 |
12 | 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 |
13 | 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 |
14 | 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. |
15 | 2007 | The role of RELN in lissencephaly and neuropsychiatric disease | Chang, B.S.; Düzcan, Füsun ; Kim, S.; Cinbis, M.; Aggarwal, A.; Apse, K.A.; Özdel, Osman İsmail |
16 | 2004 | Sister chromatid exchange frequency in lymphocytes cultured from cotton gin workers | Atmaca, Münevver; Bağcı, Hüseyin ; Açıkbaş, İbrahim ; Gümüş, Dilihan ; Düzcan, Füsun |