Rank | Title | Journal | Year | PubWeight™‹?› |
---|---|---|---|---|
1 | c. 595-596 insC of FOXC2 underlies lymphedema, distichiasis, ptosis, ankyloglossia, and Robin sequence in a Thai patient. | Am J Med Genet A | 2010 | 0.81 |
2 | Expanding the phenotypic spectrum of acro-cardio-facial syndrome (ACFS): Exclusion of P63 mutation. | Am J Med Genet A | 2009 | 0.80 |
3 | TBX22 mutation associated with cleft lip/palate, hypodontia, and limb anomaly. | Cleft Palate Craniofac J | 2011 | 0.79 |
4 | Phenotypic analysis of Arg227 mutations of TP63 with emphasis on dental phenotype and micturition difficulties in EEC syndrome. | Am J Med Genet A | 2011 | 0.78 |