| Year |
Citation |
Score |
| 2002 |
Barber TD, Barber MC, Tomescu O, Barr FG, Ruben S, Friedman TB. Identification of target genes regulated by PAX3 and PAX3-FKHR in embryogenesis and alveolar rhabdomyosarcoma. Genomics. 79: 278-84. PMID 11863357 DOI: 10.1006/Geno.2002.6703 |
0.309 |
|
| 1999 |
Liang Y, Wang A, Belyantseva IA, Anderson DW, Probst FJ, Barber TD, Miller W, Touchman JW, Jin L, Sullivan SL, Sellers JR, Camper SA, Lloyd RV, Kachar B, Friedman TB, et al. Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2. Genomics. 61: 243-58. PMID 10552926 DOI: 10.1006/Geno.1999.5976 |
0.339 |
|
| 1999 |
Barber TD, Barber MC, Cloutier TE, Friedman TB. PAX3 gene structure, alternative splicing and evolution Gene. 237: 311-319. PMID 10521655 DOI: 10.1016/S0378-1119(99)00339-X |
0.313 |
|
| 1998 |
Liang Y, Wang A, Probst FJ, Arhya IN, Barber TD, Chen KS, Deshmukh D, Dolan DF, Hinnant JT, Carter LE, Jain PK, Lalwani AK, Li XC, Lupski JR, Moeljopawiro S, et al. Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2. American Journal of Human Genetics. 62: 904-15. PMID 9529344 DOI: 10.1086/301786 |
0.361 |
|
| 1995 |
Friedman TB, Liang Y, Weber JL, Hinnant JT, Barber TD, Winata S, Arhya IN, Asher JH. A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17 Nature Genetics. 9: 86-91. PMID 7704031 DOI: 10.1038/Ng0195-86 |
0.331 |
|
| Show low-probability matches. |