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A rare intrauterine onset growth retardation syndrome caused by mosaic 19p13.3 microduplication: evaluation of GH/IGF- 1 axis and GH therapy response.
Özer, Emre; Karaman, Birsen; Günes, Nilay; Evliyaoglu, Olcay; Tüysüz, Beyhan.
Affiliation
  • Özer E; Divisions of Pediatric Genetics, Istanbul University Cerrahpasa Faculty of Medicine, Istanbul, Turkey.
  • Karaman B; Division of Medical Genetics, Istanbul University Faculty of Medicine, Istanbul, Turkey.
  • Günes N; Divisions of Pediatric Genetics, Istanbul University Cerrahpasa Faculty of Medicine, Istanbul, Turkey.
  • Evliyaoglu O; Divisions of Pediatric Endocrinology, Department of Pediatrics, Istanbul University Cerrahpasa Faculty of Medicine, Istanbul, Turkey.
  • Tüysüz B; Divisions of Pediatric Genetics, Istanbul University Cerrahpasa Faculty of Medicine, Istanbul, Turkey.
Turk J Pediatr ; 63(1): 174-180, 2021.
Article in En | MEDLINE | ID: mdl-33686842
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Intellectual Disability / Microcephaly Limits: Child / Female / Humans Language: En Journal: Turk J Pediatr Year: 2021 Document type: Article Affiliation country:
Fulltext
Add to My VHL
Print
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Intellectual Disability / Microcephaly Limits: Child / Female / Humans Language: En Journal: Turk J Pediatr Year: 2021 Document type: Article Affiliation country: