Ocular findings in 22q11.2 deletion syndrome: A systematic literature review and results of a Dutch multicenter study

Author:

Scheibler Emma N. M. M.12ORCID,Valk Bouman Emy S.3ORCID,Nuijts Myrthe A.3ORCID,Bauer Noël J. C.4ORCID,Berendschot Tos T. J. M.4ORCID,Vermeltfoort Pit5ORCID,Bok Levinus A.6ORCID,Eeghen Agnies M.178ORCID,Houben Michiel L.9,Amelsvoort Thérèse A. M. J.2ORCID,Boot Erik1210ORCID,Egmond‐Ebbeling Michelle B.3

Affiliation:

1. Advisium, 's Heeren Loo Zorggroep Amersfoort The Netherlands

2. Department of Psychiatry and Neuropsychology Maastricht University Maastricht The Netherlands

3. Department of Ophthalmology University Medical Center Utrecht Utrecht The Netherlands

4. University Eye Clinic Maastricht Maastricht University Medical Center Maastricht The Netherlands

5. Department of Ophthalmology Máxima Medical Center Veldhoven The Netherlands

6. Department of Pediatrics Máxima Medical Center Veldhoven The Netherlands

7. ENCORE, Erasmus Medical Center Rotterdam The Netherlands

8. Emma Children's Hospital University of Amsterdam Amsterdam The Netherlands

9. Department of Pediatrics, Wilhelmina Children's Hospital University Medical Center Utrecht Utrecht The Netherlands

10. The Dalglish Family 22q Clinic University Health Network Toronto Ontario Canada

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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