المؤلفون: Bolat H; Department of Medical Genetics, Balıkesir University Faculty of Medicine, Balıkesir, Turkey., Ünsel-Bolat G; Department of Child and Adolescent Psychiatry, Balıkesir University Faculty of Medicine, Balıkesir, Turkey., Derin H; Department of Pediatrics, Division of Child Neurology, Elazığ City Hospital, Balıkesir, Turkey., Şen A; Department of Medical Genetics, Firat University School of Medicine, Elazig, Turkey., Ceylaner S; Intergen Genetics Center, Ankara, Turkey.

المصدر: Molecular syndromology [Mol Syndromol] 2022 Jul; Vol. 13 (4), pp. 263-269. Date of Electronic Publication: 2022 Mar 09.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: S. Karger Country of Publication: Switzerland NLM ID: 101525192 Publication Model: Print-Electronic Cited Medium: Print ISSN: 1661-8769 (Print) Linking ISSN: 16618769 NLM ISO Abbreviation: Mol Syndromol Subsets: PubMed not MEDLINE

المؤلفون: Koç Yekedüz M; Department of Pediatric Metabolism, Children's Hospital, Ankara University Faculty of Medicine, Ankara, Turkey., Doğulu N; Department of Pediatric Metabolism, Children's Hospital, Ankara University Faculty of Medicine, Ankara, Turkey., Öncül Ü; Department of Pediatric Metabolism, Children's Hospital, Ankara University Faculty of Medicine, Ankara, Turkey., Köse E; Department of Pediatric Metabolism, Children's Hospital, Ankara University Faculty of Medicine, Ankara, Turkey., Ceylaner S; Intergen Genetics and Rare Diseases Diagnosis Research & Application Center, Ankara, Turkey., Eminoğlu FT; Department of Pediatric Metabolism, Children's Hospital, Ankara University Faculty of Medicine, Ankara, Turkey.

المصدر: Molecular syndromology [Mol Syndromol] 2022 Feb; Vol. 13 (2), pp. 146-151. Date of Electronic Publication: 2021 Oct 25.

نوع المنشور: Case Reports

بيانات الدورية: Publisher: S. Karger Country of Publication: Switzerland NLM ID: 101525192 Publication Model: Print-Electronic Cited Medium: Print ISSN: 1661-8769 (Print) Linking ISSN: 16618769 NLM ISO Abbreviation: Mol Syndromol Subsets: PubMed not MEDLINE

المؤلفون: Kisla Ekinci RM; Department of Pediatric Rheumatology, Cukurova University Faculty of Medicine, Adana, Turkey., Balci S; Department of Pediatric Rheumatology, Cukurova University Faculty of Medicine, Adana, Turkey., Dogan H; INTERGEN Genetic Diagnosis and Research Center, Ankara, Turkey., Ceylaner S; INTERGEN Genetic Diagnosis and Research Center, Ankara, Turkey., Varan C; Department of Pediatric Cardiology, Cukurova University Faculty of Medicine, Adana, Turkey., Erdem S; Department of Pediatric Cardiology, Cukurova University Faculty of Medicine, Adana, Turkey., Coban F; Department of Medical Genetics, AGENTEM, Cukurova University Faculty of Medicine, Adana, Turkey., Bisgin A; Department of Medical Genetics, AGENTEM, Cukurova University Faculty of Medicine, Adana, Turkey.

المصدر: Molecular syndromology [Mol Syndromol] 2021 Apr; Vol. 12 (2), pp. 112-117. Date of Electronic Publication: 2021 Feb 01.

نوع المنشور: Case Reports

بيانات الدورية: Publisher: S. Karger Country of Publication: Switzerland NLM ID: 101525192 Publication Model: Print-Electronic Cited Medium: Print ISSN: 1661-8769 (Print) Linking ISSN: 16618769 NLM ISO Abbreviation: Mol Syndromol Subsets: PubMed not MEDLINE

المؤلفون: Dagdeviren Cakir A; Department of Pediatric Endocrinology, Cerrahpasa Medical School, Istanbul University-Cerrahpasa, Istanbul, Turkey., Saidov S; Department of Pediatrics, Bona Dea International Hospital, Baku, Azerbaijan., Turan H; Department of Pediatric Endocrinology, Cerrahpasa Medical School, Istanbul University-Cerrahpasa, Istanbul, Turkey., Ceylaner S; Intergen Genetics Center, Ankara, Turkey., Özer Y; Department of Pediatric Endocrinology, Cerrahpasa Medical School, Istanbul University-Cerrahpasa, Istanbul, Turkey., Kutlu T; Department of Pediatric Gastroenterology, Cerrahpasa Medical School, Istanbul University-Cerrahpasa, Istanbul, Turkey., Ercan O; Department of Pediatric Endocrinology, Cerrahpasa Medical School, Istanbul University-Cerrahpasa, Istanbul, Turkey., Evliyaoglu O; Department of Pediatric Endocrinology, Cerrahpasa Medical School, Istanbul University-Cerrahpasa, Istanbul, Turkey.

المصدر: Molecular syndromology [Mol Syndromol] 2020 Jun; Vol. 11 (2), pp. 90-96. Date of Electronic Publication: 2020 Mar 18.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: S. Karger Country of Publication: Switzerland NLM ID: 101525192 Publication Model: Print-Electronic Cited Medium: Print ISSN: 1661-8769 (Print) Linking ISSN: 16618769 NLM ISO Abbreviation: Mol Syndromol Subsets: PubMed not MEDLINE

المؤلفون: Guven MA; Department of Obstetrics and Gynecology, Faculty of Medicine, Kahramanmaras Sutcu Imam University, Kahramanmaras, and Department of Genetics, Zekai Tahir Burak Women's Health Education and Research Hospital, Ankara, Turkey. mguven@ksu.edu.tr, Batukan C, Ceylaner S, Uzel M, Ozbek A, Demirpolat G

المصدر: Fetal diagnosis and therapy [Fetal Diagn Ther] 2006; Vol. 21 (4), pp. 386-9.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: S. Karger Country of Publication: Switzerland NLM ID: 9107463 Publication Model: Print Cited Medium: Print ISSN: 1015-3837 (Print) Linking ISSN: 10153837 NLM ISO Abbreviation: Fetal Diagn Ther Subsets: MEDLINE

مواضيع طبية MeSH: Ultrasonography, Prenatal*, Abnormalities, Multiple/*diagnostic imaging , Bone Diseases, Developmental/*diagnostic imaging , Craniofacial Abnormalities/*diagnostic imaging , Limb Deformities, Congenital/*diagnostic imaging , Thoracic Vertebrae/*abnormalities, Abnormalities, Multiple/pathology ; Diagnosis, Differential ; Humans ; Infant, Newborn ; Male ; Syndrome