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| 1 | Pendred syndrome,DFNB4,and PDS/SLC26A4 identification of eight novel mutation and possible genotype-phenotype correlations显示文摘 | CAMPBELL C CUCCI R A PRASAD S | 2001 | Hum Mutat2001，17，： | 1 |
| 2 | Pendred syndrome, DFNB4, and PDS/SLC26A4 i- dentification of eight novel mutations and possible genotype-phenotype correlations显示文摘 | CAMPBELL C CUCCI R A PRASAD S | 2001 | Hum Mutat2001，17，： | 1 |
| 3 | Pen- dred syndrome, DFNB4, and PDS/SLC26A4 identifi- cation of eight novel mutations and possible genotype- phenotype correlations 显示文摘 | CAMPBELL C CUCCI R A PRASAD S | 2001 | Hum Mutat2001，17，： | 1 |
| 4 | Endophthalmitis prophylaxis in cataract surgery :overview of current practice patterns in 9 European countries显示文摘 | BEHNDIG A COCHENER B GUELL JL KODJ1KIAN L MEN- CUCCI R NUIJTS RM | 2013 | J Cataract Refract Surg2013，39，9： | 1 |
| 5 | Pendred syndrome,DFNB4and PDS/SLC26A4:identification of eight novel mutations and possible genotype-phenotype correlations显示文摘 | Campbell C Cucci R Prasad S | 2001 | Hum Mutst2001，17，： | 1 |
| 6 | Pendred syndrome, DFNB4, and PDS/SLC26A4 i- dentification of eight novel mutations and possible genotype-phenotype correlations 显示文摘 | CAMPBELL C CUCCI R A PRASAD S | 2001 | Hum Mutat2001，17，： | 1 |
| 7 | Pendred syndrome and DFNB4- mutation screening of SLC26A4 by denaturing high performance liquid chromatography and the identification of eleven novehnutations显示文摘 | Prasad S K olln K A Cucci R A | 2004 | Am J Med Genet A2004，124，1： | 1 |
| 8 | Pendred syndrome and DFNB4-mutation screening of SLC26A4 by denaturing high-performance liquid chromatography and the identification of eleven novel mutations显示文摘 | PRASAD S KOLLN K A CUCCI R A | 2004 | Am J Med Genet2004，124，： | 1 |
| 9 | Particle selection,ingestion,and absorption in filter-feeding bivalves显示文摘 | Shumway S E Cucci T L Newell R C | 1985 | J Exp Mar Biol Ecol1985，91，12： | 1 |
| 10 | Particle selection,ingestion,and absorption in filter-feeding bivalves显示文摘 | SHUMWAY S E CUCCI T NEWELL R C et a1 | 1985 | J Exp Mar1985，91，： | 1 |
| 11 | Pendred Syndrome,DFNB4 and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations显示文摘 | CAMPBELL C CUCCI R A PRASAD S | 2001 | Hum Mutat2001，17，5： | 1 |
| 12 | Pendred syndrome and DFNB4-mutation screening of SLC26A4 by denaturing high-performance liquid chromatography and the identification of eleven novel mutations显示文摘 | PRASAD S KLLN K A CUCCI R A et a1 | 2004 | Am J Med Genet A2004，124，1： | 1 |
| 13 | Genetic testing for hereditary hearing loss:Connexin 26(GJB2)allele variants and two novel deafness‐causing mutations(R32Cand 645‐648delTAGA)显示文摘 | PRASAD S CUCCI R A GREEN G E | 2000 | Human Mutation2000，16，： | 1 |
| 14 | Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations 显示文摘 | Campbell C Cucci R A Prasad S | 2001 | Hum Mutat2001，17，5： | 1 |
| 15 | Pendred syndrome and DFNB4-mutation screening of SLC26A4 by denaturing high-performance liquid chromatograph and the identification of eleven novel mutations显示文摘 | PRASAD S KOLLN K A CUCCI R A | 2004 | Am J Med Genet2004，124，： | 1 |
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