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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
Results 21-26 of 26 (Search time: 0.019 seconds).
Issue Date | Title | Author(s) | |
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21 | 2005 | Prenatal diagnosis of a trisomy 13 case associated with holoprosencephaly by ultrasonography and quantitative fluorescent PCR | Şatiroğlu Tufan, N. Lale ; Tufan, Ahmet Çevik ; Yildirim, B.; Kaleli, Babür ; Semerci, C.Nur ; Bir, Ferda ; Düzcan, Füsun ; Bağcı, Hüseyin |
2 | 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 |
3 | 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. |
4 | 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 |
5 | 2006 | Sex chromosome aneuploidy rates in the somatic cells of infertile men | Düzcan, Füsun ; Aybek, Zafer. ; Tepeli, E. ; Caner, Vildan. ; Çetin, Gökhan Ozan. ; Aybek, Hülya. ; Bağcı, Hüseyin |
6 | 2004 | Sister chromatid exchange frequency in lymphocytes cultured from cotton gin workers | Atmaca, Münevver; Bağcı, Hüseyin ; Açıkbaş, İbrahim ; Gümüş, Dilihan ; Düzcan, Füsun |