Concepedia

Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice

Elizabeth A. Lindsay, Francesca Vitelli, Hong Hua Su, Masae Morishima, Tuong Huynh, Tiziano Pramparo, Vesna Jurecic, George Ogunrinu, Helen Sutherland, Peter Scambler,

Nature · 2001 · 1K citations · 20 references

DOI

Concepts

References

20

Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome

Craig T. Basson, David R. Bachinsky, Robert C. Lin et al. · Nature Genetics · 1997 · 1.1K citations

, , +16

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

Newbury-Ecob Ra, David I. Wilson, Andrew R.J. Curtis et al. · Nature Genetics · 1997 · 929 citations

, , +8

α-lnhibin is a tumour-suppressor gene with gonadal specificity in mice

Martin M. Matzuk, Milton J. Finegold, Jyan-Gwo J. Su et al. · Nature · 1992 · 890 citations

, , +11

Expression of the T-box family genes,Tbx1-Tbx5, during early mouse development

Deborah L. Chapman, Nancy Garvey, Sarah Hancock et al. · Developmental Dynamics · 1996 · 660 citations

, , +17

Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome

Michael J. Bamshad, Robert C. Lin, David Law et al. · Nature Genetics · 1997 · 546 citations

, , +12