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Boot, Erik
192
results:
Online X
Search for persons
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Format
Online (192)
Mediatypes
Articles (Online) (87)
Bookchapter (Online) (2)
OpenAccess-fulltext (103)
Languages
english (176)
spanish (1)
Sorted by: Relevance
Sorted by: Year
?
1
Dementia in Rare Genetic Neurodevelopmental Disorders: A Sy..:
Kwetsie, Hadassa
;
van Schaijk, Malu
;
Van Der Lee, Sven
...
Neurology. 102 (2024) 11 - p. , 2024
Link:
https://doi.org/10.1212/..
?
2
Prenatal cardiac findings and 22q11.2 deletion syndrome: Fe..:
Goldmuntz, Elizabeth
;
Bassett, Anne S.
;
Boot, Erik
...
Prenatal Diagnosis. 44 (2024) 6-7 - p. 804-814 , 2024
Link:
https://doi.org/10.1002/..
?
3
Navigating the outcome maze: a scoping review of outcomes a..:
Müller, Annelieke R.
;
van Silfhout, Nadia Y.
;
den Hollander, Bibiche
...
Therapeutic Advances in Rare Disease. 5 (2024) - p. , 2024
Link:
https://doi.org/10.1177/..
?
4
Psychiatric and neurological manifestations in adults with ..:
Korteling, Dorinde
;
Musch, Jiska L. I.
;
Zinkstok, Janneke R.
.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 195 (2023) 2 - p. , 2023
Link:
https://doi.org/10.1002/..
?
5
Updated clinical practice recommendations for managing chil..:
Óskarsdóttir, Sólveig
;
Boot, Erik
;
Crowley, Terrence Blaine
...
Genetics in Medicine. 25 (2023) 3 - p. 100338 , 2023
Link:
https://doi.org/10.1016/..
?
6
Optometry in adults with microdeletion 22q11.2: The eye as ..:
von Scheibler, Emma N.M.M.
;
Appaji, Abhishek
;
Berendschot, Tos T.J.M.
...
Biomarkers in Neuropsychiatry. 9 (2023) - p. 100081 , 2023
Link:
https://doi.org/10.1016/..
?
7
P112: Updated clinical practice guidelines for managing chi..:
Bassett, Anne
;
Oskarsdottir, Solveig
;
Boot, Erik
.
Genetics in Medicine Open. 1 (2023) 1 - p. 100141 , 2023
Link:
https://doi.org/10.1016/..
?
8
Intellectual and Behavioral Phenotypes of Smith–Magenis Syn..:
Linders, Cathelijne C.
;
van Eeghen, Agnies M.
;
Zinkstok, Janneke R.
..
Genes. 14 (2023) 8 - p. 1514 , 2023
Link:
https://doi.org/10.3390/..
?
9
Hearing loss and history of otolaryngological conditions in..:
von Scheibler, Emma N. M. M.
;
Widdershoven, Josine C. C.
;
van Barneveld, Denise C. P. B. M.
...
American Journal of Medical Genetics Part A. 194 (2023) 3 - p. , 2023
Link:
https://doi.org/10.1002/..
?
10
Prenatal Screening and Diagnostic Considerations for 22q11...:
Blagowidow, Natalie
;
Nowakowska, Beata
;
Schindewolf, Erica
...
Genes. 14 (2023) 1 - p. 160 , 2023
Link:
https://doi.org/10.3390/..
?
11
Approaches to studying the impact of 22q11.2 copy number va..:
Bassett, Anne S.
;
McDonald-McGinn, Donna M.
;
Boot, Erik
..
The American Journal of Human Genetics. 110 (2023) 7 - p. 1216-1218 , 2023
Link:
https://doi.org/10.1016/..
?
12
Updated clinical practice recommendations for managing adul..:
Boot, Erik
;
Óskarsdóttir, Sólveig
;
Loo, Joanne C.Y.
...
Genetics in Medicine. 25 (2023) 3 - p. 100344 , 2023
Link:
https://doi.org/10.1016/..
?
13
Parkinsonism in Genetic Neurodevelopmental Disorders: A Sys..:
von Scheibler, Emma N.M.M.
;
van Eeghen, Agnies M.
;
de Koning, Tom J.
...
Movement Disorders Clinical Practice. 10 (2022) 1 - p. 17-31 , 2022
Link:
https://doi.org/10.1002/..
?
14
Post-traumatic stress in adults with 22q11.2 deletion syndr..:
von Scheibler, Emma N. M. M.
;
van Amelsvoort, Thérèse A. M. J.
;
Vingerhoets, Claudia
..
BJPsych Open. 8 (2022) 4 - p. , 2022
Link:
https://doi.org/10.1192/..
?
15
Contributors:
, In:
The Chromosome 22q11.2 Deletion Syndrome
,
Bassett, Anne S.
;
Van Batavia, Jason P.
;
Boot, Erik
... - p. xv-xvii , 2022
Link:
https://doi.org/10.1016/..
1-15