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The Relationship between Genotype and Phenotype in Primary Ciliary Dyskinesia Patients

dc.contributor.authorÇEBİ, Memnune Nur
dc.contributor.authorÇOKUĞRAŞ, Haluk Cezmi
dc.contributor.authorOcak, Zeynep
dc.contributor.authorKILINÇ SAKALLI, Ayşe Ayzıt
dc.date.accessioned2021-12-10T10:19:54Z
dc.date.available2021-12-10T10:19:54Z
dc.date.issued2021
dc.identifier.citationKILINÇ SAKALLI A. A. , ÇEBİ M. N. , Ocak Z., ÇOKUĞRAŞ H. C. , "The Relationship between Genotype and Phenotype in Primary Ciliary Dyskinesia Patients", MEDICAL BULLETIN OF SISLI ETFAL HOSPITAL, cilt.55, sa.2, ss.188-192, 2021
dc.identifier.othervv_1032021
dc.identifier.otherav_39404ee7-0c4b-4260-9747-35d2fd33ebe8
dc.identifier.urihttp://hdl.handle.net/20.500.12627/169689
dc.identifier.urihttps://doi.org/10.14744/semb.2020.22567
dc.description.abstractObjectives: Primary ciliary dyskinesia (PCD) is a chronic genetic disease that affects the respiratory tract, characterized by different clinical and laboratory features. It has a very difficult diagnosis, and high morbidity. In recent years, with the advances in genetics, the rate of diagnosis has increased considerably. In this study, it was aimed to evaluate the relationship between PCD patients' clinical, radiological and laboratory features and genetic analysis.
dc.language.isoeng
dc.subjectFamily Practice
dc.subjectFundamentals and Skills
dc.subjectGeneral Health Professions
dc.subjectPathophysiology
dc.subjectInternal Medicine
dc.subjectAssessment and Diagnosis
dc.subjectMedicine (miscellaneous)
dc.subjectGeneral Medicine
dc.subjectHealth Sciences
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectTIP, GENEL & İÇECEK
dc.titleThe Relationship between Genotype and Phenotype in Primary Ciliary Dyskinesia Patients
dc.typeMakale
dc.relation.journalMEDICAL BULLETIN OF SISLI ETFAL HOSPITAL
dc.contributor.departmentİstanbul Üniversitesi-Cerrahpaşa , Cerrahpaşa Tıp Fakültesi , Dahili Tıp Bilimleri Bölümü
dc.identifier.volume55
dc.identifier.issue2
dc.identifier.startpage188
dc.identifier.endpage192
dc.contributor.firstauthorID2693222


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