3 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
| 1 | 17176450 | A novel HLA-DRB1*11 allele, DRB1*1155, was found in a patient through routine DRB1 typing using sequence-specific primers (SSP) and confirmed by allele-specific sequence-based typing. | 2006 Dec | 1 |
| 2 | 10484981 | Hereditary TP53 codon 292 and somatic P16INK4A codon 94 mutations in a Li-Fraumeni syndrome family. | 1999 Sep | 1 |
| 3 | 8880573 | A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans. | 1996 Sep | 1 |