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| 1 | The complex genetics of Kallmann syndrome: KAL1, FGFR1, FGF8, ROKR2, PROK2, et al 显示文摘 | HARDELIN JP DODE C | 2008 | Sex Dev2008，2，8： | 1 |
| 2 | KCNQ4,a K+ channel mutated in a form of dominant deafness,is expressed in the inner ear and the central auditory pathway显示文摘 | Kharkovets T Hardelin J P Safieddine S | 2000 | Proc Natl Acad Sci U S A2000，97，8： | 1 |
| 3 | The complex genetics of Kallmann syndrome KALl, FCFRI , FCF8, PROKR2, PROK2 显示文摘 | HARDELIN J P DODE C | 2008 | Sex Dev2008，2，45： | 1 |
| 4 | KCNQ4 ,a K^+ channel mutatek in foum of dominant deaf- ness,is expressed in the central auditory pathway 显示文摘 | KHARKOVETS T HARDELIN J P SAFIEDDINE S | 2000 | Proc Natl Acad Sci USA2000，97，8： | 1 |
| 5 | Molecular genetics of hearing loss 显示文摘 | Petit C Levilliers J Hardelin JP | 2001 | Annu Rev Genet2001，35，： | 1 |
| 6 | Molecular genetics of hearing loss显示文摘 | Petit C Levilliers J Hardelin JP | 2001 | Annu Rev Genet2001，35，： | 1 |
| 7 | The complex genetics of Kallmann syndrome:KAL1,FGFR1,FGF8,PROKR2,PROK2,et al显示文摘 | Hardelin JP Dodé C | | 0，，4： | 1 |
| 8 | 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 |
| 9 | The Complex genetics of Kallmann syndrome: KAL1 ,FGFR1 ,FGF8 ,PROKR2, PROK2 显示文摘 | Hardelin JP Dode C | 2008 | Sex Dev2008，2，45： | 1 |
| 10 | Hereditary deafness:Molecular genetics 显示文摘 | Hardelin JP Denoyelle F Levilliers J | 2004 | Med Sci (Paris)2004，20，3： | 1 |
| 11 | Kallmann syndrome显示文摘 | Dodé C Hardelin JP | 2009 | Eur J Hum Genet2009，17，2： | 1 |
| 12 | KCNQ4, a K+ channel mutated in a form of dominant deafness ,is expressed in the inner ear and the central auditory pathway显示文摘 | Kharkovets T Hardelin JP Safieddine S | 2000 | Proc Natl Acad Sci USA2000，97，8： | 1 |
| 13 | Kallmann syndrome显示文摘 | Dode C Hardelin JP | 2009 | Eur J Hum Genet2009，17，2： | 1 |
| 14 | Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome显示文摘 | Hardelin JP Levilliers J Blanchard S | 1993 | Hum Mol Genet1993，2，4： | 1 |
| 15 | KCNQ4,a K+ channel mutated in a form of dominant deafness,is expressed in the inner ear and the central auditory pathway显示文摘 | Kharkovets T Hardelin JP Safieddine S | 2000 | Proc Nail Acad Sci U S A2000，97，： | 1 |
| 16 | Kallmann syndrome:fibroblast growth factor signaling insufficiency?显示文摘 | Dode C Hardelin J P | 2004 | J Mol Med(Berl)2004，82，11： | 1 |
| 17 | X-chromosome linked Kallmann syndrome:stop mutations validate the candidate gene显示文摘 | Hardelin JP Levilliers J del Castillo I | 1992 | Proc Natl Acad Sci USA1992，89，17： | 1 |
| 18 | Molecular genetics of hearing loss显示文摘 | Petit C Levilliers J Hardelin JP | 2001 | Annu Rev Genet2001，35，12： | 1 |
| 19 | Kallmann syndrome:towards molecular pathogenesis显示文摘 | Hardelin JP | 2001 | Mol Cell Endocrinol2001，179，12： | 1 |
| 20 | Kallmann syndrome Towards molecular pathogenesis 显示文摘 | Hardelin JP | 2001 | Mol Cell Endocrinol2001，179，12： | 1 |
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