المؤلفون: Xiaochuan Long, Li Chen, Xinyao Xiao, Xiayu Min, Yao Wu, Zengming Yang, Xin Wen

المصدر: Frontiers in Cell and Developmental Biology, Vol 12 (2024)

مصطلحات موضوعية: primary cilia, reproductive physiology, ciliary diseases, Hh signaling pathway, Wnt signaling pathway, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fcell.2024.1418928/full; https://doaj.org/toc/2296-634X

URL الوصول: https://doaj.org/article/f9dbcd6d7c8c4d2db89ee6df6db44951

المؤلفون: KARADAĞ, BÜLENT TANER

المساهمون: Eksi D. D., Yilmaz E., Basaran A. E., ERDURAN G., NUR B., MIHÇI E., KARADAĞ B. T., BİNGÖL A., Alper O. M.

مصطلحات موضوعية: Tıp, Sağlık Bilimleri, Dahili Tıp Bilimleri, Çocuk Sağlığı ve Hastalıkları, Medicine, Health Sciences, Internal Medicine Sciences, Child Health and Diseases, PEDİATRİ, Klinik Tıp, Klinik Tıp (MED), PEDIATRICS, CLINICAL MEDICINE, Clinical Medicine (MED), Perinatology and Child Health, Primary ciliary dyskinesia, Targeted next-generation sequencing, Mutation analysis, Ciliary diseases, DIAGNOSIS, MUTATIONS, CCDC40

وصف الملف: application/pdf

Relation: INDIAN JOURNAL OF PEDIATRICS; Eksi D. D., Yilmaz E., Basaran A. E., ERDURAN G., NUR B., MIHÇI E., KARADAĞ B. T., BİNGÖL A., Alper O. M., "Novel Gene Variants Associated with Primary Ciliary Dyskinesia", INDIAN JOURNAL OF PEDIATRICS, cilt.89, sa.7, ss.682-691, 2022; 691; 682; https://pubmed.ncbi.nlm.nih.gov/35239159/; https://hdl.handle.net/11424/287645; 89

الاتاحة: https://hdl.handle.net/11424/287645
https://doi.org/10.1007/s12098-022-04098-z
https://pubmed.ncbi.nlm.nih.gov/35239159/

المؤلفون: Durkadin Demir Eksi, Elanur Yilmaz, A. Erdem Basaran, Gizem Erduran, Banu Nur, Ercan Mihci, Bulent Karadag, Aysen Bingol, Ozgul M. Alper

المساهمون: Eksi D. D., Yilmaz E., Basaran A. E., ERDURAN G., NUR B., MIHÇI E., KARADAĞ B. T., BİNGÖL A., Alper O. M.

مصطلحات موضوعية: Sağlık Bilimleri, DIAGNOSIS, Pediatrics, Clinical Medicine (MED), Çocuk Sağlığı ve Hastalıkları, Child Health and Diseases, Cohort Studies, Primary ciliary dyskinesia, Health Sciences, Humans, CCDC40, Klinik Tıp (MED), Targeted next-generation sequencing, Genetic Association Studies, Ciliary diseases, Internal Medicine Sciences, Klinik Tıp, Kartagener Syndrome, MUTATIONS, High-Throughput Nucleotide Sequencing, Dahili Tıp Bilimleri, CLINICAL MEDICINE, Tıp, Mutation analysis, Mutation, Pediatrics, Perinatology and Child Health, Medicine, PEDİATRİ

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::559621d1e5f2e6ea19c412c44d68a243
https://hdl.handle.net/11424/287645