1. A mutation in TGFB3 associated with a syndrome of low muscle mass, growth retardation, distal arthrogryposis and clinical features overlapping with marfan and loeys–dietz syndrome. Issue 8 (3rd July 2013) Authors: Rienhoff, Hugh Young; Yeo, Chang‐Yeol; Morissette, Rachel; Khrebtukova, Irina; Melnick, Jonathan; Luo, Shujun; Leng, Nan; Kim, Yeon‐Jin; Schroth, Gary; Westwick, John; Vogel, Hannes; McDonnell, Nazli; Hall, Judith G.; Whitman, Malcolm Journal: American journal of medical genetics Issue: Volume 161:Issue 8(2013:Aug.) Page Start: 2040 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Analysis of growth factor signaling in embryos. (©2007) Other Names: Whitman, Malcolm; Sater, Amy Katherine, 1959- Record Type: Book Extent: 1 online resource (435 pages), illustrations View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Loss of Vlk in Prx1+ Cells Delays the Initial Steps of Endochondral Bone Formation and Fracture Repair in the Limb. (16th February 2022) Authors: Maridas, David E; Gamer, Laura; Moore, Emily R; Doedens, Annemiek M; Yu, Yunqing; Ionescu, Andreia; Revollo, Leila; Whitman, Malcolm; Rosen, Vicki Journal: Journal of bone and mineral research Issue: Volume 37:Number 4(2022) Page Start: 764 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗