Page 86 - Characterization of genetic neurodevelopmental disorders at adult age, with a focus on 22q11.2 deletion syndrome - Emma Boersma
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Chapter 2
sTable 1. continued
Study specifications
Search
date study
number
First author Publication
year
Journal Publication
type
Countries of
study
166
167 Hetzelt167 2021 Eur j med genet Article Germany
168 Nomura168 2021 Brain dev-jpn Article Japan
169 Araujo169 2020 Movement disord Article Brazil
170 Lesage170 2021 Front neurol Article France
170
170
170
171 Krebs171 2013 Hum mutat Article U.S.A.
171
172 Quadri172 2013 Hum mutat Article Italy
172
173 Olgiati173 2014 Neurogenetics Article Italy
173
174 Kirola174 2016 Parkinsonism relat d Article India
174
175 Taghavi175 2018 Mol neurobiol Article Iran
175
176 Ben Romdhan176 2018 J mol neurosci Article Tunisia
176
177 Hong177 2019 Parkinsonism relat d Article China
177
178 Xie178 2019 Parkinsonism relat d Article China
178
Light blue: identified through cross-reference check. Orange: overlap in study population with
other studies but additional information provided (patients were only included once in the review).
Abbreviations: U.S.A.=United States of America, U.K.=United Kingdom, y=years, m=months, d=days.
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