RUNX2mutations in Taiwanese patients with cleidocranial dysplasia

Genetics and Molecular Biology

Volumn 34, Issue 2, 2011, Pages 201-204

  Lin, Wei De ^a,b   Lin, Shuan Pei ^c   Wang, Chung Hsing ^a   Tsai, Yushin ^b   Chen, Chih Ping ^c   Tsai, Fuu Jen ^a,b,d  

^a CHINA MEDICAL UNIVERSITY HOSPITAL   (Taiwan)

^b CHINA MEDICAL UNIVERSITY   (Taiwan)

^c MACKAY MEMORIAL HOSPITAL   (Taiwan)

^d ASIA UNIVERSITY   (Taiwan)

Author keywords

CCD; Cleidocranial dysplasia; RUNX2; RUNX2 deletion mutation

Indexed keywords

TRANSCRIPTION FACTOR RUNX2;

3' UNTRANSLATED REGION; ADULT; ALLELE; ARTICLE; CHILD; CLEIDOCRANIAL DYSPLASIA; CLINICAL ARTICLE; ETHNIC GROUP; EXON; FEMALE; GENE DELETION; GENE DOSAGE; GENE MUTATION; GENE SEQUENCE; HETEROZYGOSITY; HUMAN; MALE; MISSENSE MUTATION; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; POINT MUTATION; PRESCHOOL CHILD; PROMOTER REGION; REAL TIME POLYMERASE CHAIN REACTION; RUNX2 GENE; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; TAIWANESE;

EID: 79957909600     PISSN: 14154757     EISSN: 16784685     Source Type: Journal    
DOI: 10.1590/S1415-47572011005000002     Document Type: Article

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