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| 1 | Histologic findings after amniotic membrane graft in the human cornea 显示文摘 | Gris O Wolley Dod C Guell JL | 2002 | Ophthalmology2002，109，3： | 1 |
| 2 | Clinical signifcance of P46L and R92Q substitutions in the tumour necrosis factor superfamily 1A gene显示文摘 | Ravet N Rouaghe S Dodé C | 2006 | Ann Rheum Dis2006，65，： | 1 |
| 3 | Kallmann syndrome caused by mutations in the PROK2 and PROKR2 genes:pathophysiology and genotype-phenotype correlations显示文摘 | Sarfati J Dodé C Young J | | 0，，： | 1 |
| 4 | The complex genetics of Kallmann syndrome:KAL1,FGFR1,FGF8,PROKR2,PROK2,et al显示文摘 | Hardelin JP Dodé C | | 0，，4： | 1 |
| 5 | The complex genetics of Kallmann syndrome:KAL1,FGFR1,FGFg,PROKR2,PROK2,et al显示文摘 | Hardelin JP Dodé C | 2008 | Sex Dev2008，2，45： | 1 |
| 6 | Loss-of-function muta- tions in FGFR 1 cause autosomal dominant Kallmann syn- drome显示文摘 | Dod C Levilliers J Dupont JM eta/ | 2003 | Nat Genet2003，33，4： | 1 |
| 7 | Kallmann syndrome显示文摘 | Dodé C Hardelin JP | 2009 | Eur J Hum Genet2009，17，2： | 1 |
| 8 | Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome显示文摘 | Dodé C Levilliers J Dupont JM | 2003 | Nat Genet2003，33，4： | 1 |
| 9 | Kallmann syndrome:mutations in the genes encoding prokineticin-2 and prokineticin receptor2显示文摘 | Dodé C Teixeira L Levilliers J | 2006 | PLoS Genet2006，2，10： | 1 |
| 10 | The ubiquitous solar electric propulsion stage显示文摘 | Austin R E Dod R E Terwilliger C H | 1977 | Acta Astronautica1977，4，1： | 1 |
| 11 | Kallmann syndrome:mutations in the genes encoding prokineticin-2 and prokineticin receptor-2显示文摘 | DOD C TEIXEIRA L LEVILLIERS J | 2006 | PLo S Genet2006，2，10： | 1 |
| 12 | Kallmann syndrome:mutations in the genes encoding prokineticin-2 and prokineticin receptor-2显示文摘 | Dodé C Teixeira L Levilliers J | 2006 | PLoS Genetics2006，2，10： | 1 |
| 13 | Kallmann syndrome: mutations in the genes eneoding prokinetiein-2 and prokinetiein receptor-2显示文摘 | Dod C Teixeira L Levilliers J | 2006 | PLoS Genet2006，2，10： | 1 |
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