Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
Details
Serval ID
serval:BIB_0A97B223441B
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
Journal
American Journal of Human Genetics
Publication state
Published
Issued date
2020
Language
english
Publisher's website
Create date
18/10/2024 14:04
Last modification date
25/10/2024 14:58