Concepedia

Examination of FGFRL1 as a candidate gene for diaphragmatic defects at chromosome 4p16.3 shows that Fgfrl1 null mice have reduced expression of Tpm3, sarcomere genes and Lrtm1 in the diaphragm

Nelson D. LopezJimenez, Simon Gerber, Vlad Popovici, Sonia Mirza, Kirsten A. Copren, Linda Ta, Gary M. Shaw, Beat Trüeb, Anne Slavotinek

Human Genetics · 2009 · 29 citations · 64 references

DOIFull text

Open access

Concepts

References

64

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

Lisenka E.L.M. Vissers, Conny M.A. van Ravenswaaij, R.J.C. Admiraal et al. · Nature Genetics · 2004 · 1.3K citations

, , +4

Hypertrophic Cardiomyopathy

Pascale Richard, Philippe Charron, Lucie Carrier et al. · Circulation · 2003 · 1.3K citations · Full text

, , +14

Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse

Chris D. Vulpe, Yien–Ming Kuo, Therese L. Murphy et al. · Nature Genetics · 1999 · 1.1K citations

, , +16

Fibroblast Growth Factor Receptor 3 Is a Negative Regulator of Bone Growth

Anthony Wynshaw‐Boris, Fen Zhou, Ann Kuo et al. · Cell · 1996 · 1.1K citations · Full text

, , +12

Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3

Jennifer S. Colvin, Barbara A. Bohne, Gary W. Harding et al. · Nature Genetics · 1996 · 869 citations

, , +14