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Journal description
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Details for article 1 of 12 found articles
| Title: |
A higher rare CNV burden in the genetic background potentially contributes to intellectual disability phenotypes in 22q11.2 deletion syndrome |
| Author: |
Jensen, Matthew Kooy, R. Frank Simon, Tony J. Reyniers, Edwin Girirajan, Santhosh Tassone, Flora |
| Appeared in: |
European journal of medical genetics |
| Paging: | Volume 61 (2018) nr. 4 pages 209-212 |
| Year: |
2018 |
| Contents: | |
| Publisher: |
Published by Elsevier B.V. |
| Source file: |
Elektronische Wetenschappelijke Tijdschriften |
Details for article 1 of 12 found articles
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