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All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year Sort by creator [A → Z]' creator [Z → A]' publishing year ↑ (asc)' publishing year ↓ (desc)' title [A → Z]' title [Z → A]' Simple Search Hits 1 – 5 of 5 1 Speech and language phenotype in Phelan-McDermid (22q13.3) syndrome Brignell, Amanda; Gu, Conway; Holm, Alison... In: Eur J Hum Genet (2020) BASE Show details 2 Deep phenotyping of speech and language skills in individuals with 16p11.2 deletion Mei, Cristina; Fedorenko, Evelina; Amor, David J.. - : Springer International Publishing, 2018 BASE Show details 3 Further clinical and molecular delineation of the 15q24 microdeletion syndrome Mefford, Heather C; Rosenfeld, Jill A; Shur, Natasha. - : British Medical Journal Publishing Group, 2012 BASE Show details 4 Further clinical and molecular delineation of the 15q24 microdeletion syndrome Mefford, Heather C; Rosenfeld, Jill A; Shur, Natasha. - : British Medical Journal Publishing Group, 2011 BASE Show details 5 A genotype-first approach for the molecular and clinical characterization of uncommon de novo microdeletion of 20q13.33 Traylor, Ryan N.; Bruno, Damien L.; Burgess, Trent. - : Public Library of Science, 2010 BASE Show details

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