Mutation of the gene encoding fibrillin-2 results in syndactyly in mice

Human Molecular Genetics

Volumn 10, Issue 8, 2001, Pages 835-843

  Chaudhry, Shazia S ^a   Gazzard, James ^b   Baldock, Clair ^a   Dixon, Jill ^a   Rock, Matthew J ^a   Skinner, Gail C ^a   Steel, Karen P ^b   Kielty, Cay M ^a   Dixon, Michael J ^a  

^a UNIVERSITY OF MANCHESTER   (United Kingdom)

^b MRC INSTITUTE OF HEARING RESEARCH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

COLLAGEN FIBRIL; CYSTEINE; FIBRILLIN; GLYCOPROTEIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARACHNODACTYLY; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BONE DISEASE; CARDIOVASCULAR DISEASE; CHROMOSOME 15Q; CHROMOSOME 5Q; CLUSTER ANALYSIS; COLLAGEN DISEASE; CONGENITAL MALFORMATION; CONTROLLED STUDY; DISEASE SEVERITY; EAR MALFORMATION; ELASTICITY; EXON; EYE DISEASE; FIBER; FINGER MALFORMATION; GENE MUTATION; GENETIC ANALYSIS; HOMEOSTASIS; JOINT CONTRACTURE; MARFAN SYNDROME; MOUSE; MOUSE MUTANT; NEWBORN DISEASE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; SYNDACTYLY;

ANIMALIA;

EID: 0035311574     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/10.8.835     Document Type: Article

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