Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice

BMC Developmental Biology

Volumn 14, Issue 1, 2014, Pages

  Motch Perrine, Susan M ^a   Cole, Theodore M ^b   Martínez Abadías, Neus ^a,e   Aldridge, Kristina ^c   Jabs, Ethylin Wang ^d   Richtsmeier, Joan T ^a,f  

^a PENNSYLVANIA STATE UNIVERSITY   (United States)

^b UNIVERSITY OF MISSOURI KANSAS CITY SCHOOL OF MEDICINE   (United States)

^c University of Missouri   (United States)

^d MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^e CENTRE FOR GENOMIC REGULATION CRG   (Spain)

^f JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Apert syndrome; Cranial development; Craniosynostosis; Fibroblast growth factor receptor signaling; Skull growth; Suture

Indexed keywords

FGFR2 PROTEIN, MOUSE; FIBROBLAST GROWTH FACTOR RECEPTOR 2;

ACROCEPHALOSYNDACTYLY; ANIMAL; ARTICLE; C57BL MOUSE; CONGENITAL MALFORMATION; CRANIAL SUTURE; CRANIOFACIAL MALFORMATION; FETUS DEVELOPMENT; GENETICS; HUMAN; METABOLISM; MOUSE; MUTATION; NEWBORN; PRENATAL DEVELOPMENT; PRINCIPAL COMPONENT ANALYSIS; TIME; TRANSGENIC MOUSE;

ACROCEPHALOSYNDACTYLIA; ANIMALS; ANIMALS, NEWBORN; CRANIAL SUTURES; CRANIOFACIAL ABNORMALITIES; FETAL DEVELOPMENT; HUMANS; MICE; MICE, INBRED C57BL; MICE, TRANSGENIC; MUTATION; PRINCIPAL COMPONENT ANALYSIS; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 2; TIME FACTORS;

MUS;

EID: 84900506749     PISSN: None     EISSN: 1471213X     Source Type: Journal    
DOI: 10.1186/1471-213X-14-8     Document Type: Article

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