| | Title | Authors / Editors | Date |
|
unige:137334 |
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects |
Zhao, Yingjie; Diacou, Alexander; Johnston, H Richard; Musfee, Fadi I; ... Morrow, Bernice E |
2020 |
|
unige:138349 |
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion |
Cleynen, Isabelle; Engchuan, Worrawat; Hestand, Matthew S; Heung, Tracy; ... Bassett, Anne S |
2020 |
|
unige:132729 |
Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11.2 deletion syndrome |
Niarchou, Maria; Chawner, Samuel J R A; Fiksinski, Ania; Vorstman, Jacob A S; ... Thapar, Anita |
2019 |
|
unige:102778 |
Deletion size analysis of 1,680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2 |
Guo, Tingwei; Diacou, Alexander; Hiroko, Nomaru; McDonald-McGinn, Donna M; ... Morrow, Bernice E |
2018 |
|
unige:126967 |
Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects |
Zhao, Yingjie; Guo, Tingwei; Fiksinski, Ania; Breetvelt, Elemi; ... Morrow, Bernice E |
2018 |
Emanuel, Beverly S
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