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Volumn 12, Issue 4, 1996, Pages 485-490

Molecular basis of congenital bilateral absence of the vas deferens;LE GENE CFTR: AGENESIE DES DEFERENTS ET MUCOVISCIDOSE, DEUX MALADIES POUR UN MEME GENE

Author keywords

[No Author keywords available]

Indexed keywords

TRANSMEMBRANE CONDUCTANCE REGULATOR;

EID: 0029865710     PISSN: 07670974     EISSN: None     Source Type: Journal    
DOI: 10.4267/10608/767     Document Type: Review
Times cited : (5)

References (22)
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    • Population variation of Common Cystic Fibrosis Mutations
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  • 8
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    • Analysis of the whole CFTR coding regions and splice junctions in azoospermic men with congenital bilateral aplasia of epididymis or vas deferens
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    • Mercier, B.1    Verlingue, C.2    Lissons, W.3    Silber, F.4    Novelli, G.5    Bonduelle, M.6    Audrézet, M.P.7    Férec, C.8
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    • Maladies de Tay-Sachs et de Sandhoff. Les déficits en β-hexosaminidases, modèles des maladies des lysosomes
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.