Marino, BrunoRefine your research by the most used items
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- Breckpot, Jeroen (3)
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- Philip, Nicole (3)
- Swillen, Ann (3)
- Armando, Marco (2)
- Bassett, Anne S (2)
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remove all| Title | Authors / Editors | Date | |
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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 |
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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 |
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Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome | Mlynarski, Elisabeth E.; Xie, Michael; Taylor, Deanne; Sheridan, Molly B.; ... Emanuel, Beverly S. | 2016 |
