Craniofacial malformations: Intrinsic vs extrinsic neural crest cell defects in Treacher Collins and 22q11 deletion syndromes

Clinical Genetics

Volumn 69, Issue 6, 2006, Pages 471-479

  Walker, M B ^a   Trainor, Paul A ^a  

^a STOWERS INSTITUTE FOR MEDICAL RESEARCH   (United States)

Author keywords

22q11 deletion syndrome; Collins syndrome; Congenital birth defects; Craniofacial; Neural crest cells

Indexed keywords

BONE MORPHOGENETIC PROTEIN 2; FIBROBLAST GROWTH FACTOR; NOTCH RECEPTOR; WNT PROTEIN;

CELL DIFFERENTIATION; CELL MIGRATION; CELL PROLIFERATION; CHROMOSOME 22Q; CHROMOSOME DELETION; CRANIOFACIAL DEVELOPMENT; DIGEORGE SYNDROME; ECTODERM; EMBRYO DEVELOPMENT; ENDODERM; GASTRULATION; HUMAN; INCIDENCE; MANDIBULOFACIAL DYSOSTOSIS; MESODERM; NERVOUS SYSTEM DEVELOPMENT; NEURAL CREST CELL; NONHUMAN; PATHOGENESIS; PRIORITY JOURNAL; REVIEW; SIGNAL TRANSDUCTION;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; HUMANS; MANDIBULOFACIAL DYSOSTOSIS; NEURAL CREST;

VERTEBRATA;

EID: 33646812163     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.0009-9163.2006.00615.x     Document Type: Review

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