The phenotypic overlap of syndromes associated with hereditary gingival fibromatosis: follow-up of a family for five years

Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology and Endodontology

Volumn 103, Issue 4, 2007, Pages 521-527

  Haytac, M Cenk ^a   Ozcelik, Onur ^a  

^a CUKUROVA UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; CHILD; FAMILY; FEMALE; GENETICS; GINGIVA FIBROMATOSIS; HUMAN; HYPERTRICHOSIS; LONGITUDINAL STUDY; MALE; MENTAL DEFICIENCY; MIDDLE AGED; MULTIPLE MALFORMATION SYNDROME; NEWBORN; PATHOLOGY; PHENOTYPE; PRESCHOOL CHILD; SYNDROME;

ABNORMALITIES, MULTIPLE; ADOLESCENT; CHILD; CHILD, PRESCHOOL; FAMILY; FEMALE; FIBROMATOSIS, GINGIVAL; HUMANS; HYPERTRICHOSIS; INFANT, NEWBORN; LONGITUDINAL STUDIES; MALE; MENTAL RETARDATION; MIDDLE AGED; PHENOTYPE; SYNDROME;

EID: 33947511580     PISSN: 10792104     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tripleo.2006.02.021     Document Type: Article

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