Mutations in the Gene Encoding Capillary Morphogenesis Protein 2 Cause Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis
The American Journal of Human Genetics2003Vol. 73(4), pp. 791–800
Citations Over TimeTop 10% of 2003 papers
Sandra Hanks, Sarah Adams, Jenny Douglas, Laura Arbour, David J. Atherton, Sevim Balcı, Harald Bode, Mary Ellen Campbell, Murray Feingold, Gökhan Keser, Wim J. Kleijer, Grazia M.S. Mancini, John A. McGrath, Francesco Muntoni, Arti Nanda, M. Dawn Teare, Matthew L. Warman, F. Michael Pope, Andrea Superti‐Furga, P. Andrew Futreal, Nazneen Rahman
Related Papers
- → Morphomechanical programming of morphogenesis in Cnidarian embryos(2006)31 cited
- → Ovarian Fibromas With Heavy Deposition of Hyaline Globules: a Diagnostic Pitfall(2009)16 cited
- → “Hyaline droplet” formation and some other adrenocortical changes following methylandrostenediol treatment in the rat(1963)6 cited
- [Trypsic inhibitors in serum and hyaline membrane disease (author's transl)].(1977)