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Volumn 121, Issue 3 PART1, 2013, Pages 142-147

Novel RUNX2 frameshift mutations in Chinese patients with cleidocranial dysplasia

Author keywords

Cleidocranial dysplasia; Dental abnormalities; Frameshift mutation; Runt related transcription factor 2

Indexed keywords

RUNX2 PROTEIN, HUMAN; TRANSCRIPTION FACTOR RUNX2;

EID: 84877681093     PISSN: 09098836     EISSN: 16000722     Source Type: Journal    
DOI: 10.1111/eos.12048     Document Type: Article
Times cited : (10)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.