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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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20
0
false
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20
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false
Subject
- 1 45X karyotype
- 1 Abnormal Karyotype
- 1 Abnormalities, Multiple
- 1 Abortion, Spontaneous
- 1 academic achievement
- 1 Adolescent
- 1 age distribution
- 1 Age Factors; Age of Onset; Child; Color Perception; Disease Progression; Female; Genes, Dominant; Genetic Linkage; Hearing Loss, Sensorineural/*genetics/physiopathology; Humans; Male; Microsatellite Repeats; Optic Atrophy, Autosomal Dominant/*genetics/physiopathology; Pedigree; Recombination, Genetic; Turkey/epidemiology
- 1 agyria
- 1 Albright syndrome
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Date issued
Type
- 23 Article
Fulltext
Results 21-23 of 23 (Search time: 0.014 seconds).
Issue Date | Title | Author(s) | |
---|---|---|---|
21 | 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. |
22 | 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 |
23 | 2004 | Sister chromatid exchange frequency in lymphocytes cultured from cotton gin workers | Atmaca, Münevver; Bağcı, Hüseyin ; Açıkbaş, İbrahim ; Gümüş, Dilihan ; Düzcan, Füsun |