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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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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 |
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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 |
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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 |
