Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
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| Description | scientific article published on 20 December 2019 |
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author: Joris R Vermeesch Maude Schneider Stephan Eliez Maria Pontillo Carrie E Bearden Wendy R Kates Thérèse A.M.J. Van Amelsvoort Marco Armando Marta Unolt Elizabeth Goldmuntz |
| Publication date | December 20, 2019 |
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