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Ocular findings in 22q11.2 deletion syndrome: A systematic literature review and results of a Dutch multicenter study.
von Scheibler, Emma N M M; van der Valk Bouman, Emy S; Nuijts, Myrthe A; Bauer, Noël J C; Berendschot, Tos T J M; Vermeltfoort, Pit; Bok, Levinus A; van Eeghen, Agnies M; Houben, Michiel L; van Amelsvoort, Thérèse A M J; Boot, Erik; van Egmond-Ebbeling, Michelle B.
Afiliación
  • von Scheibler ENMM; Advisium, 's Heeren Loo Zorggroep, Amersfoort, The Netherlands.
  • van der Valk Bouman ES; Department of Psychiatry and Neuropsychology, Maastricht University, Maastricht, The Netherlands.
  • Nuijts MA; Department of Ophthalmology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Bauer NJC; Department of Ophthalmology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Berendschot TTJM; University Eye Clinic Maastricht, Maastricht University Medical Center, Maastricht, The Netherlands.
  • Vermeltfoort P; University Eye Clinic Maastricht, Maastricht University Medical Center, Maastricht, The Netherlands.
  • Bok LA; Department of Ophthalmology, Máxima Medical Center, Veldhoven, The Netherlands.
  • van Eeghen AM; Department of Pediatrics, Máxima Medical Center, Veldhoven, The Netherlands.
  • Houben ML; Advisium, 's Heeren Loo Zorggroep, Amersfoort, The Netherlands.
  • van Amelsvoort TAMJ; ENCORE, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Boot E; Emma Children's Hospital, University of Amsterdam, Amsterdam, The Netherlands.
  • van Egmond-Ebbeling MB; Department of Pediatrics, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
Am J Med Genet A ; 188(2): 569-578, 2022 02.
Article en En | MEDLINE | ID: mdl-34773366
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías del Ojo / Síndrome de DiGeorge / Discapacidad Intelectual Tipo de estudio: Clinical_trials / Diagnostic_studies / Guideline / Observational_studies / Prevalence_studies / Risk_factors_studies / Systematic_reviews Límite: Adolescent / Adult / Child / Child, preschool / Humans / Infant / Middle aged / Newborn Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Países Bajos
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías del Ojo / Síndrome de DiGeorge / Discapacidad Intelectual Tipo de estudio: Clinical_trials / Diagnostic_studies / Guideline / Observational_studies / Prevalence_studies / Risk_factors_studies / Systematic_reviews Límite: Adolescent / Adult / Child / Child, preschool / Humans / Infant / Middle aged / Newborn Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Países Bajos