Bibliographic Details
| Title: |
Loeys–Dietz syndrome caused by 1q41 deletion including TGFB2 is associated with a neurodevelopmental phenotype |
| Authors: |
Fry, Deanna, Groepper, Daniel, MacCarrick, Gretchen, Demo, Erin M., Thomas, Matthew J., Wilkes, Margaret J., Lyons, Michael J., Tucker, Megan E., Steding, Catherine, Fleischer, Julie |
| Source: |
American journal of medical genetics.Part A. 188(7):2237-2241 |
| Availability: |
http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100153540427.0x000001&indx=1&recIds=ETOCvdc_100153540427.0x000001 |
| Database: |
British Library Document Supply Centre Inside Serials & Conference Proceedings |
