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1دورية أكاديمية
المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı., orcid:0000-0003-0710-5422, orcid:0000-0003-4402-9609, Sağlam, Halil, Erdöl, Şahin, Dorum, Sevil, C-7392-2019, 35612700100, 54419947800, 41661166200
مصطلحات موضوعية: Endocrinology & metabolism, Pediatrics, Hypophosphatasia, Turkish children, Alkaline-phosphatase gene, Mutations, Adult, Child, Female, Genotype, Humans, Male, Retrospective studies, Turkey, Asfotase Alfa, Alkaline Phosphatase, Adolescent, ALPL gene, Article, Assisted ventilation, Autosomal recessive disorder, Bone mineralization, Bone radiography, Chest circumference, Clinical article, Clinical assessment, Controlled study, Deciduous tooth, DNA sequence, Dual energy X ray absorptiometry
وصف الملف: application/pdf
العلاقة: Makale - Uluslararası Hakemli Dergi; 2016-19/13; JCRPE Journal of Clinical Research in Pediatric Endocrinology; Sağlam, H. vd. (2017). ''Clinical and genetic findings of Turkish hypophosphatasia cases''. JCRPE Journal of Clinical Research in Pediatric Endocrinology, 9(3), 229-236.; https://doi.org/10.4274/jcrpe.4549Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596804Test/; http://hdl.handle.net/11452/30547Test; 000410406300007; 2-s2.0-85029042566; 229; 236
الإتاحة: https://doi.org/10.4274/jcrpe.4549Test
http://hdl.handle.net/11452/30547Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596804Test/ -
2دورية أكاديمية
المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı., orcid:0000-0003-0710-5422, orcid:0000-0003-4402-9609, Sağlam, Halil, Erdöl, Şahin, Dorum, Sevil, C-7392-2019, 35612700100, 54419947800, 41661166200
مصطلحات موضوعية: Endocrinology & metabolism, Pediatrics, Hypophosphatasia, Turkish children, Alkaline-phosphatase gene, Mutations, Adult, Child, Female, Genotype, Humans, Male, Retrospective studies, Turkey, Asfotase Alfa, Alkaline Phosphatase, Adolescent, ALPL gene, Article, Assisted ventilation, Autosomal recessive disorder, Bone mineralization, Bone radiography, Chest circumference, Clinical article, Clinical assessment, Controlled study, Deciduous tooth, DNA sequence, Dual energy X ray absorptiometry
وصف الملف: application/pdf
العلاقة: Makale - Uluslararası Hakemli Dergi; 2016-19/13; JCRPE Journal of Clinical Research in Pediatric Endocrinology; Sağlam, H. vd. (2017). ''Clinical and genetic findings of Turkish hypophosphatasia cases''. JCRPE Journal of Clinical Research in Pediatric Endocrinology, 9(3), 229-236.; https://doi.org/10.4274/jcrpe.4549Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596804Test/; http://hdl.handle.net/11452/30547Test; 000410406300007; 2-s2.0-85029042566; 229; 236
الإتاحة: https://doi.org/10.4274/jcrpe.4549Test
http://hdl.handle.net/11452/30547Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596804Test/
النص الكامل