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A Girl With Beckwith-Wiedemann Syndrome and Pseudohypoparathyroidism Type 1B Due to Multiple Imprinting Defects.
Bakker, Boudewijn; Sonneveld, Laura J H; Woltering, M Claire; Bikker, Hennie; Kant, Sarina G.
Affiliation
  • Bakker B; Department of Pediatrics (B.B., L.J.H.S., M.C.W.), Reinier de Graaf Hospital, 2625 AD Delft, The Netherlands; Department of Clinical Genetics (H.B.), Academic Medical Center, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands; and Department of Clinical Genetics (S.G.K.), Leiden University
  • Sonneveld LJ; Department of Pediatrics (B.B., L.J.H.S., M.C.W.), Reinier de Graaf Hospital, 2625 AD Delft, The Netherlands; Department of Clinical Genetics (H.B.), Academic Medical Center, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands; and Department of Clinical Genetics (S.G.K.), Leiden University
  • Woltering MC; Department of Pediatrics (B.B., L.J.H.S., M.C.W.), Reinier de Graaf Hospital, 2625 AD Delft, The Netherlands; Department of Clinical Genetics (H.B.), Academic Medical Center, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands; and Department of Clinical Genetics (S.G.K.), Leiden University
  • Bikker H; Department of Pediatrics (B.B., L.J.H.S., M.C.W.), Reinier de Graaf Hospital, 2625 AD Delft, The Netherlands; Department of Clinical Genetics (H.B.), Academic Medical Center, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands; and Department of Clinical Genetics (S.G.K.), Leiden University
  • Kant SG; Department of Pediatrics (B.B., L.J.H.S., M.C.W.), Reinier de Graaf Hospital, 2625 AD Delft, The Netherlands; Department of Clinical Genetics (H.B.), Academic Medical Center, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands; and Department of Clinical Genetics (S.G.K.), Leiden University
J Clin Endocrinol Metab ; 100(11): 3963-6, 2015 Nov.
Article in En | MEDLINE | ID: mdl-26367199
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pseudohypoparathyroidism / Beckwith-Wiedemann Syndrome / Down-Regulation / Genomic Imprinting / DNA Methylation / Epigenesis, Genetic Type of study: Etiology_studies Limits: Female / Humans / Infant Language: En Journal: J Clin Endocrinol Metab Year: 2015 Document type: Article Country of publication: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pseudohypoparathyroidism / Beckwith-Wiedemann Syndrome / Down-Regulation / Genomic Imprinting / DNA Methylation / Epigenesis, Genetic Type of study: Etiology_studies Limits: Female / Humans / Infant Language: En Journal: J Clin Endocrinol Metab Year: 2015 Document type: Article Country of publication: United States