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Volumn 2, Issue 11, 2001, Pages 831-

Human genetics: Closing in on palatal disorders

(1)  Casci, Tanita a  

a NONE

Author keywords

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Indexed keywords


EID: 84984934108     PISSN: 14710056     EISSN: 14710064     Source Type: Journal    
DOI: 10.1038/35098519     Document Type: Article
Times cited : (2)

References (2)
  • 1
    • 0034785350 scopus 로고    scopus 로고
    • The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate andankyloglossia
    • Braybrook, C. The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate andankyloglossia. Nature Genet. 29, 179-183 (2001)
    • (2001) Nature Genet. , vol.29 , pp. 179-183
    • Braybrook, C.1
  • 2
    • 0034789530 scopus 로고    scopus 로고
    • Mutation of PVRL1 is associated with sporadic non-syndromic cleftlip/palate in northern Venezuela
    • Sozen, M. A. Mutation of PVRL1 is associated with sporadic non-syndromic cleftlip/palate in northern Venezuela. Nature Genet. 29, 141-142 (2001)
    • (2001) Nature Genet. , vol.29 , pp. 141-142
    • Sozen, M.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.