[Clinical and image features, and identification of pathogenic gene mutation of two cleidocranial dysplasia families].

Zhonghua er ke za zhi. Chinese journal of pediatrics

Volumn 48, Issue 11, 2010, Pages 834-838

  Wang, Guang xin ^a   Ma, Li xia ^b   Xu, Wan feng ^b   Song, Feng ling ^b   Sun, Ruo peng ^b  

^a SHANDONG UNIVERSITY   (China)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

RUNX2 PROTEIN, HUMAN; TRANSCRIPTION FACTOR RUNX2;

ARTICLE; CHILD; CLEIDOCRANIAL DYSPLASIA; EXON; FEMALE; GENETICS; HUMAN; MALE; MUTATION; NUCLEOTIDE SEQUENCE; PATHOLOGY; PEDIGREE; PHENOTYPE; PRESCHOOL CHILD;

CHILD; CHILD, PRESCHOOL; CLEIDOCRANIAL DYSPLASIA; CORE BINDING FACTOR ALPHA 1 SUBUNIT; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; HUMANS; MALE; MUTATION; PEDIGREE; PHENOTYPE;

EID: 80155201447     PISSN: 05781310     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)