Diverse clinical and genetic aspects of craniofrontonasal syndrome

Pediatric Neurology

Volumn 44, Issue 2, 2011, Pages 83-87

  Zafeiriou, Dimitrios I ^a   Pavlidou, Efterpi L ^a   Vargami, Euthymia ^a  

^a ARISTOTLE UNIVERSITY OF THESSALONIKI   (Greece)

Author keywords

[No Author keywords available]

Indexed keywords

BODY DYSMORPHIC DISORDER; COMPUTER ASSISTED TOMOGRAPHY; CRANIOFACIAL MALFORMATION; CRANIOFACIAL SYNOSTOSIS; CRANIOFRONTONASAL SYNDROME; EXON; FACE MALFORMATION; GENE DELETION; GENETIC ANALYSIS; GENETIC COUNSELING; GENOTYPE PHENOTYPE CORRELATION; HUMAN; HYPERTELORISM; INHERITANCE; MIDLINE DEFECT SYNDROME; PRIORITY JOURNAL; REVIEW; X CHROMOSOME INACTIVATION;

ANIMALS; CRANIOFACIAL ABNORMALITIES; FEMALE; GENOTYPE; HUMANS; MALE; MUTATION; PHENOTYPE;

EID: 79251548948     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2010.10.012     Document Type: Review

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