Mice mutant for Egfr and Shp2 have defective cardiac semilunar valvulogenesis
Nature Genetics2000Vol. 24(3), pp. 296–299
Citations Over TimeTop 10% of 2000 papers
Binbin Chen, Roderick T. Bronson, Lori D. Klaman, Thomas Hampton, Jufeng Wang, Patricia J. Green, Terry Magnuson, Pamela S. Douglas, James P. Morgan, Benjamin G. Neel
Related Papers
- → The penetrance of rare variants in cardiomyopathy-associated genes: A cross-sectional approach to estimating penetrance for secondary findings(2023)61 cited
- → Penetrance of LGI1 mutations in autosomal dominant partial epilepsy with auditory features(2008)67 cited
- → Co‐occurrence of hypertrophic cardiomyopathy and myeloproliferative disorder in a neonate with Noonan syndrome carrying Thr73Ile mutation in PTPN11(2015)5 cited
- → Penetrance of Fra(X) gene: Influence of grandparental origin of the gene, mental status of the carrier mother, and presence of a normal transmitting male(1992)8 cited
- Loss of heterozygosity for YNZ22 loci in human ovarian carcinomas(1999)