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Investigation of (Epi)genetic causes in syndromic short children born small for gestational age.
Tüysüz, Beyhan; Kasap, Büsra; Uludag Alkaya, Dilek; Alp Ünkar, Zeynep; Köseoglu, Pinar; Geyik, Filiz; Özer, Emre; Önal, Hasan; Gezdirici, Alper; Ercan, Oya.
Afiliação
  • Tüysüz B; Department of Pediatric Genetics, Istanbul University-Cerrahpasa, Cerrahpasa Medical Faculty, Istanbul, Turkey. Electronic address: beyhan@iuc.edu.tr.
  • Kasap B; Department of Pediatric Genetics, Istanbul University-Cerrahpasa, Cerrahpasa Medical Faculty, Istanbul, Turkey.
  • Uludag Alkaya D; Department of Pediatric Genetics, Istanbul University-Cerrahpasa, Cerrahpasa Medical Faculty, Istanbul, Turkey.
  • Alp Ünkar Z; Department of Neonatology, Istanbul University-Cerrahpasa, Cerrahpasa Medical Faculty, Istanbul, Turkey.
  • Köseoglu P; Department of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Turkey.
  • Geyik F; Department of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Turkey.
  • Özer E; Department of Pediatric Genetics, Istanbul University-Cerrahpasa, Cerrahpasa Medical Faculty, Istanbul, Turkey.
  • Önal H; Department of Pediatric Endocrinology, University of Health Sciences Turkey, Basaksehir Çam ve Sakura City Hospital, Istanbul, Turkey.
  • Gezdirici A; Department of Medical Genetic, University of Health Sciences Turkey, Basaksehir Çam ve Sakura City Hospital, Istanbul, Turkey.
  • Ercan O; Department of Pediatric Endocrinology, Istanbul University-Cerrahpasa, Cerrahpasa Medical Faculty, Istanbul, Turkey.
Eur J Med Genet ; 66(11): 104854, 2023 Nov.
Article em En | MEDLINE | ID: mdl-37758162
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Nanismo Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Child / Humans / Newborn Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Nanismo Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Child / Humans / Newborn Idioma: En Ano de publicação: 2023 Tipo de documento: Article