A Chinese girl with cleidocranial dysplasia (CCD) caused by the recurrent R190W mutation in RUNX 2

Zhonghua er ke za zhi. Chinese journal of pediatrics

Volumn 42, Issue 10, 2004, Pages 759-761

  Qiu, Zheng qing ^a   Tang, Ai lan ^a   Yu, Wei ^a   Ao, Yang ^a   Wilson, H Y ^a   Wei, Min ^a   Zhang, Xue ^a  

^a PEKING UNION MEDICAL COLLEGE HOSPITAL   (China)

Author keywords

[No Author keywords available]

Indexed keywords

RUNX2 PROTEIN, HUMAN; TRANSCRIPTION FACTOR RUNX2;

ARTICLE; CASE REPORT; CLEIDOCRANIAL DYSPLASIA; FEMALE; GENETICS; HUMAN; MUTATION;

CLEIDOCRANIAL DYSPLASIA; CORE BINDING FACTOR ALPHA 1 SUBUNIT; FEMALE; HUMANS; MUTATION;

EID: 77951999381     PISSN: 05781310     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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