Your browser doesn't support javascript.
loading
Aberrant DNA methylation as a diagnostic biomarker of diabetic embryopathy.
Schulze, Katharina V; Bhatt, Amit; Azamian, Mahshid S; Sundgren, Nathan C; Zapata, Gladys E; Hernandez, Patricia; Fox, Karin; Kaiser, Jeffrey R; Belmont, John W; Hanchard, Neil A.
Afiliación
  • Schulze KV; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Bhatt A; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
  • Azamian MS; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Sundgren NC; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
  • Zapata GE; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
  • Hernandez P; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
  • Fox K; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Kaiser JR; Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, TX, USA.
  • Belmont JW; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
  • Hanchard NA; Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, TX, USA.
Genet Med ; 21(11): 2453-2461, 2019 11.
Article en En | MEDLINE | ID: mdl-30992551

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Metilación de ADN / Diabetes Mellitus / Enfermedades Fetales Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Infant / Newborn / Pregnancy Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Metilación de ADN / Diabetes Mellitus / Enfermedades Fetales Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Infant / Newborn / Pregnancy Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos