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 TitleAuthors / EditorsDate
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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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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