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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
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Status
Former staff
Subject
- 1 Adolescent
- 1 adolescent
- 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 article
- 1 astigmatism
- 1 autosomal recessive inheritance
- 1 Bardet Biedl syndrome
- 1 brachydactyly
- 1 case report
- 1 Cervix Uteri
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Type
- 2 Article
Fulltext
Results 1-2 of 2 (Search time: 0.007 seconds).
Issue Date | Title | Author(s) | |
---|---|---|---|
1 | 2002 | Laurence-Moon-Biedl syndrome with vaginal atresia | Kara, İnci Gökalan ; Düzcan, Füsun ; Aktan, Erdal |
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 |