A novel single-base deletion in ROR2 causes atypical brachydactyly type B1 with cutaneous syndactyly in a large Chinese family

Journal of Human Genetics

Volumn 54, Issue 7, 2009, Pages 422-425

  Lv, Dan ^a   Luo, Yang ^b   Yang, Wei ^a   Cao, Lihua ^b   Wen, Yaran ^a   Zhao, Xiuli ^a   Sun, Miao ^a   Lo, Wilson H Y ^a   Zhang, Xue ^a,c  

^a PEKING UNION MEDICAL COLLEGE   (China)

^b CHINA MEDICAL UNIVERSITY   (China)

^c INSTITUTE OF BASIC MEDICAL SCIENCES   (China)

Author keywords

Brachydactyly type B1; Deletion; ROR2; Syndactyly

Indexed keywords

POLYPEPTIDE; PROTEIN TYROSINE KINASE; RECEPTOR TYROSINE KINASE LIKE ORPHAN RECEPTOR 2; UNCLASSIFIED DRUG;

ARTICLE; BRACHYDACTYLY; BRACHYDACTYLY TYPE B1; CARBOXY TERMINAL SEQUENCE; CHINESE; CUTANEOUS SYNDACTYLY; GENE DELETION; GENE LOCUS; GENE MUTATION; GENETIC LINKAGE; HUMAN; PHENOTYPE; SYNDACTYLY;

ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CHINA; DNA MUTATIONAL ANALYSIS; FAMILY; FEMALE; HUMANS; MALE; MOLECULAR SEQUENCE DATA; PEDIGREE; RECEPTOR TYROSINE KINASE-LIKE ORPHAN RECEPTORS; SEQUENCE DELETION; SKIN ABNORMALITIES; SYNDACTYLY;

EID: 68449098664     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1038/jhg.2009.48     Document Type: Article

References (13)

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