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Proceedings of the National Academy of Sciences of the United States of America

Volumn 98, Issue 7, 2001, Pages 3855-3860

A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffersyndrome-like phenotypes

(4) Hajihosseini, Mohammad K a,b Wilson, Stephen a De Moerlooze, Laurence a,c Dickson, Clive a

a IMPERIAL CANCER RESEARCH FUND (United Kingdom)

b UNIVERSITY OF BIRMINGHAM (United Kingdom)

c GLAXOSMITHKLINE BIOLOGICALS (Belgium)

Author keywords

Craniosynostosis; Kidney; Lacrimal gland; Lung; Sternum

Indexed keywords

FIBROBLAST GROWTH FACTOR;

ACROCEPHALOSYNDACTYLY; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; CRANIOFACIAL SYNOSTOSIS; DEATH; EXON; EXOPHTHALMOS; FEMALE; GENE EXPRESSION; GENE MUTATION; GROWTH RETARDATION; HEMIZYGOTE; MALE; MOUSE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; RNA SPLICING; SYNDROME; SYNOSTOSIS;

ACROCEPHALOSYNDACTYLIA; ANIMALS; BONE DISEASES, DEVELOPMENTAL; BRAIN; CARTILAGE; CRANIAL SUTURES; EXONS; FEMALE; GENE DELETION; MICE; MICE, INBRED C57BL; OSSIFICATION, HETEROTOPIC; PHENOTYPE; RECEPTOR PROTEIN-TYROSINE KINASES; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 2; RECEPTORS, FIBROBLAST GROWTH FACTOR; VISCERA;

ANIMALIA;

EID: 0035957343 PISSN: 00278424 EISSN: None Source Type: Journal
DOI: 10.1073/pnas.071586898 Document Type: Article

Times cited : (144)

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