Evolution of the face in Loeys-Dietz syndrome type II: Longitudinal observations from infancy in seven cases

Clinical Dysmorphology

Volumn 17, Issue 4, 2008, Pages 243-248

  Adès, Lesley C ^a,b  

^a UNIVERSITY OF SYDNEY   (Australia)

^b Department of Clinical Genetics ^*  (Australia)

Author keywords

Arterial aneurysms; Craniofacial phenotype; Loeys dietz syndrome ii

Indexed keywords

ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; FACE DEVELOPMENT; FACE DYSMORPHIA; FACIES; FEMALE; FOLLOW UP; GENE; GENE MUTATION; HUMAN; INFANT; MALE; MALFORMATION SYNDROME; PRIORITY JOURNAL; TGFBR1 GENE; TGFBR2 GENE;

ADULT; AORTIC ANEURYSM; CHILD; CHILD, PRESCHOOL; CRANIOFACIAL ABNORMALITIES; FACE; FEMALE; FOLLOW-UP STUDIES; HUMANS; MALE; MAXILLOFACIAL DEVELOPMENT; MUTATION; PEDIGREE; PROTEIN-SERINE-THREONINE KINASES; RECEPTORS, TRANSFORMING GROWTH FACTOR BETA; SYNDROME;

EID: 55349129650     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/MCD.0b013e328303e5d3     Document Type: Article

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