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An investigation of the etiology and follow-up findings in 35 children with overgrowth syndromes, including biallelic SUZ12 variant.
Yüksel Ülker, Aylin; Uludag Alkaya, Dilek; Çaglayan, Ahmet Okay; Usluer, Esra; Aykut, Ayça; Aslanger, Ayça; Vural, Mehmet; Tüysüz, Beyhan.
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  • Yüksel Ülker A; Department of Pediatric Genetics, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey.
  • Uludag Alkaya D; Department of Pediatric Genetics, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey.
  • Çaglayan AO; Departments of Neurosurgery, Neurobiology and Genetics, Yale School of Medicine, New Haven, Connecticut, USA.
  • Usluer E; Department of Pediatric Genetics, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey.
  • Aykut A; Department of Medical Genetics, Faculty of Medicine, Ege University, Izmir, Turkey.
  • Aslanger A; Department of Medical Genetics, Bezmialem University, Istanbul, Turkey.
  • Vural M; Department of Neonatology, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey.
  • Tüysüz B; Department of Pediatric Genetics, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey.
Am J Med Genet A ; 191(6): 1530-1545, 2023 06.
Article en En | MEDLINE | ID: mdl-36919607
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Factores de Transcripción / Discapacidad Intelectual Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Humans Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article País de afiliación: Turquía
Texto completo
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XML
PubMed Links
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Factores de Transcripción / Discapacidad Intelectual Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Humans Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article País de afiliación: Turquía