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http://hub.abes.fr/oup/periodical/hmg/1994/volume_3/issue_12/101093hmg3122163/authorship/12
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An Entity of Type :
vivo:Authorship
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scienceplus.abes.fr
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Service de Genetique Medicale, Clinique Chirurgicale Infantile et Unite de Recherches sur les Handicaps Genetques de I1 Enfant, INSERM U-393, Hdprtal Necker-Enfants Malades
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Munnich Arnold
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12
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Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene
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