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Investigation of (epi)genotype causes and follow-up manifestations in the patients with classical and atypical phenotype of Beckwith-Wiedemann spectrum.
Tüysüz, Beyhan; Günes, Nilay; Geyik, Filiz; Yesil, Gözde; Celkan, Tiraje; Vural, Mehmet.
Affiliation
  • Tüysüz B; Istanbul University-Cerrahpasa Cerrahpasa, Medical School, Department of Pediatric Genetics, Istanbul, Turkey.
  • Günes N; Istanbul University-Cerrahpasa Cerrahpasa, Medical School, Department of Pediatric Genetics, Istanbul, Turkey.
  • Geyik F; Istanbul University-Cerrahpasa Cerrahpasa, Medical School, Department of Pediatric Genetics, Istanbul, Turkey.
  • Yesil G; Istanbul University, Aziz Sancar Experimental Medicine Research Institute Department of Genetics, Istanbul, Turkey.
  • Celkan T; Bezmialem University Medical School, Department of Medical Genetics, Istanbul, Turkey.
  • Vural M; Istanbul University-Cerrahpasa, Cerrahpasa Medical School, Department of Pediatric Hematology/ Oncology, Istanbul, Turkey.
Am J Med Genet A ; 185(6): 1721-1731, 2021 06.
Article in En | MEDLINE | ID: mdl-33704912
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Full text: 1 Database: MEDLINE Main subject: Beckwith-Wiedemann Syndrome / Genomic Imprinting / DNA Methylation / Cyclin-Dependent Kinase Inhibitor p57 Type of study: Etiology_studies Limits: Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2021 Type: Article Affiliation country: Turkey
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Full text: 1 Database: MEDLINE Main subject: Beckwith-Wiedemann Syndrome / Genomic Imprinting / DNA Methylation / Cyclin-Dependent Kinase Inhibitor p57 Type of study: Etiology_studies Limits: Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2021 Type: Article Affiliation country: Turkey