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UnknownEnhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes.
Not available
S-EPMC3591861 | biostudies-literature
UnknownCognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome.
Not available
S-EPMC4383767 | biostudies-literature
UnknownGenetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.
Not available
S-EPMC7396297 | biostudies-literature
UnknownUsing common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome.
Not available
S-EPMC7975627 | biostudies-literature
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