| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Partial deletion of ANKRD11 results in the KBG phenotype distinct from the 16q24.3 microdeletion syndrome. | Am J Med Genet A | 2013 | 0.88 |
| 2 | A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity. | Genet Med | 2012 | 0.86 |
| 3 | Constitutional trisomy 8 mosaicism due to meiosis II non-disjunction in a phenotypically normal woman with hematologic abnormalities. | Am J Med Genet A | 2004 | 0.84 |
| 4 | Histiocytic sarcoma transdifferentiated from follicular lymphoma presenting as a cutaneous tumor. | J Cutan Pathol | 2011 | 0.84 |
| 5 | CD5-negative, CD10-negative small B-cell leukemia: variant of chronic lymphocytic leukemia or a distinct entity? | Am J Hematol | 2002 | 0.81 |
| 6 | Autosomal dominant congenital cataract in a Libyan Jewish family: cosegregation with a reciprocal chromosomal translocation [t(3;5)(p22.3; p15.1)]. | Mol Vis | 2008 | 0.78 |