|
Volumn 33, Issue 2, 2011, Pages 147-152
|
[Mutation analysis of the pathogenic gene in a Chinese family with Brachydactyly type B1].
|
Author keywords
[No Author keywords available]
|
Indexed keywords
RECEPTOR TYROSINE KINASE LIKE ORPHAN RECEPTOR;
ROR2 PROTEIN, HUMAN;
ADOLESCENT;
ADULT;
AMINO ACID SEQUENCE;
ANIMAL;
ARTICLE;
ASIAN;
CHEMISTRY;
CHILD;
CHINA;
FEMALE;
FOOT MALFORMATION;
GENETICS;
HAND MALFORMATION;
HUMAN;
MALE;
MIDDLE AGED;
MISSENSE MUTATION;
MOLECULAR GENETICS;
NUCLEOTIDE SEQUENCE;
PEDIGREE;
POINT MUTATION;
PRESCHOOL CHILD;
SEQUENCE ALIGNMENT;
ADOLESCENT;
ADULT;
AMINO ACID SEQUENCE;
ANIMALS;
ASIAN CONTINENTAL ANCESTRY GROUP;
BASE SEQUENCE;
CHILD;
CHILD, PRESCHOOL;
CHINA;
FEMALE;
FOOT DEFORMITIES, CONGENITAL;
HAND DEFORMITIES, CONGENITAL;
HUMANS;
MALE;
MIDDLE AGED;
MOLECULAR SEQUENCE DATA;
MUTATION, MISSENSE;
PEDIGREE;
POINT MUTATION;
RECEPTOR TYROSINE KINASE-LIKE ORPHAN RECEPTORS;
SEQUENCE ALIGNMENT;
YOUNG ADULT;
|
EID: 79955949347
PISSN: 02539772
EISSN: None
Source Type: Journal
DOI: 10.3724/SP.J.1005.2011.00147 Document Type: Article |
Times cited : (4)
|
References (0)
|