Goldmuntz, ElizabethRefine your research by the most used items
Author / Editor
- Breckpot, Jeroen (2)
- Eliez, Stéphan (2)
- Gothelf, Doron (2)
- Marino, Bruno (2)
- Philip, Nicole (2)
- Swillen, Ann (2)
- Zackai, Elaine (2)
- Agopian, A J (1)
- Armando, Marco (1)
- Bassett, Anne S (1)
Document type
Full text accessibility
Full text version
Subject
Highlights
Show items per page
remove all| Title | Authors / Editors | Date | |
|---|---|---|---|
 |
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 |
|
|
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 |
