Cleidocranial dysplasia syndrome: Clinical characteristics and mutation study of a chinese family

International Journal of Clinical and Experimental Medicine

Volumn 6, Issue 10, 2013, Pages 900-907

  Wang, Shengguo ^a   Zhang, Shu ^a   Wang, Yanmin ^b   Chen, Yangxi ^b   Zhou, Li ^b  

^a CHONGQING MEDICAL UNIVERSITY   (China)

^b SICHUAN UNIVERSITY   (China)

Author keywords

Cleidocranial dysplasia syndrome; Family; Genetic analysis

Indexed keywords

GENOMIC DNA;

ADOLESCENT; ARTICLE; BONE DYSPLASIA; CASE REPORT; CBFA1 GENE; CHINESE; CLEIDOCRANIAL DYSPLASIA; CLINICAL FEATURE; CRANIAL ENLARGEMET; EXON; FAMILIAL DISEASE; FEMALE; GENE; GENE MUTATION; GENETIC ANALYSIS; HIP DYSPLASIA; HUMAN; MUTATIONAL ANALYSIS; NASAL BONE; PERIODONTAL DISEASE; RUNX2 GENE; SCOLIOSIS; SHORT STATURE; SKULL DISEASE; TOOTH DISEASE;

EID: 84887853496     PISSN: None     EISSN: 19405901     Source Type: Journal    
DOI: None     Document Type: Article

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