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Congenital anomalies and genetic disorders in neonates and infants: a single-center observational cohort study.
Marouane, A; Olde Keizer, R A C M; Frederix, G W J; Vissers, L E L M; de Boode, W P; van Zelst-Stams, W A G.
Affiliation
  • Marouane A; Department of Human Genetics, Radboud University Medical Center, Radboud Institute of Health Sciences, Nijmegen, The Netherlands.
  • Olde Keizer RACM; Department of Health Sciences and Primary Care, University Medical Center, Utrecht, The Netherlands.
  • Frederix GWJ; Department of Human Genetics, Radboud University Medical Center, Radboud Institute of Health Sciences, Nijmegen, The Netherlands.
  • Vissers LELM; Department of Health Sciences and Primary Care, University Medical Center, Utrecht, The Netherlands.
  • de Boode WP; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • van Zelst-Stams WAG; Department of Neonatology, Radboudumc Amalia Children's Hospital, Radboud Institute of Health Sciences, Nijmegen, the Netherlands.
Eur J Pediatr ; 181(1): 359-367, 2022 Jan.
Article in En | MEDLINE | ID: mdl-34347148
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Intensive Care Units, Neonatal / Genetic Testing Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans / Infant / Newborn Language: En Journal: Eur J Pediatr Year: 2022 Document type: Article Affiliation country:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Intensive Care Units, Neonatal / Genetic Testing Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans / Infant / Newborn Language: En Journal: Eur J Pediatr Year: 2022 Document type: Article Affiliation country: