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Modern Rheumatology Volume 25, 2015 - Issue 2
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Case Report

Coexistence of two rare genetic disorders: Kartagener syndrome and familial Mediterranean fever

Deniz ÇetinDivision of Rheumatology, Department of Internal Medicine, Adnan Menderes University Faculty of Medicine, Aydin, TurkeyCorrespondence[email protected]
,
Beyza Genç ÇetinDivision of Rheumatology, Department of Internal Medicine, Adnan Menderes University Faculty of Medicine, Aydin, Turkey
,
Taşkın ŞentürkDivision of Rheumatology, Department of Internal Medicine, Adnan Menderes University Faculty of Medicine, Aydin, Turkey
,
Songül Şahin ÇildağDivision of Rheumatology, Department of Internal Medicine, Adnan Menderes University Faculty of Medicine, Aydin, Turkey
&
İkbal Yılmaz AkdamDivision of Rheumatology, Department of Internal Medicine, Adnan Menderes University Faculty of Medicine, Aydin, Turkey
Pages 312-314 | Received 04 Dec 2012, Accepted 22 Mar 2013, Published online: 18 Feb 2014

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Dhandayuthapani Sudha, Irene Rosita Pia Patric, Aparna Ganapathy, Smitha Agarwal, Shuba Krishna, Srividya Neriyanuri, Sarangapani Sripriya, Parveen Sen, Subbulakshmi Chidambaram & Jayamuruga Pandian Arunachalam. (2017) Genetic studies in a patient with X-linked retinoschisis coexisting with developmental delay and sensorineural hearing loss. Ophthalmic Genetics 38:3, pages 260-266.
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Articles from other publishers (3)

Salem Bouomrani, Ines Masmoudi & Sawssan Ben Teber. (2020) Familial Mediterranean fever: What associations to screen for?. Rheumatology 58:3, pages 150-154.
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Adam J. Shapiro, Maimoona A. Zariwala, Thomas Ferkol, Stephanie D. Davis, Scott D. Sagel, Sharon D. Dell, Margaret Rosenfeld, Kenneth N. Olivier, Carlos Milla, Sam J. Daniel, Adam J. Kimple, Michele Manion, Michael R. Knowles & Margaret W. Leigh. (2015) Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art review. Pediatric Pulmonology 51:2, pages 115-132.
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Mahmut Cerkez Ergoren, Rameez Hassan Pirzada, Mustafa Arici & Nedime Serakinci. (2015) Near East University Genetic Mutation Database (NEU-GD): The first mutation database of Northern Cyprus. Gene 571:1, pages 145-148.
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