Rank | Title | Journal | Year | PubWeight™‹?› |
---|---|---|---|---|
1 | Combined occurrence of Alström syndrome and bronchiectasis. | Pediatrics | 2014 | 0.87 |
2 | Unbalanced 3;22 translocation with 22q11 and 3p deletion syndrome. | Am J Med Genet A | 2010 | 0.87 |
3 | Frank-ter Haar syndrome with unusual clinical features. | Eur J Med Genet | 2009 | 0.84 |
4 | Association of endothelial nitric oxide synthase gene polymorphisms (894G/T, -786T/C, G10T) and clinical findings in patients with migraine. | Neuromolecular Med | 2014 | 0.78 |
5 | A novel insertion mutation identified in exon 10 of the MEFV gene associated with Familial Mediterranean Fever. | BMC Med Genet | 2014 | 0.77 |
6 | Holoprosencephaly: ZIC2 mutation in a case with panhypopituitarism. | J Pediatr Endocrinol Metab | 2014 | 0.75 |