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Volumn 108, Issue 3, 2009, Pages

KBG syndrome: review of the literature and findings of 5 affected patients

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BONE; CASE REPORT; CEPHALOMETRY; CHILD; CONGENITAL MALFORMATION; CRANIOFACIAL MALFORMATION; DWARFISM; FEMALE; FOLLOW UP; GENETICS; HUMAN; INCISOR; MALE; MALOCCLUSION; MENTAL DEFICIENCY; MULTIPLE MALFORMATION SYNDROME; PATHOLOGY; PRESCHOOL CHILD; SYNDROME; TOOTH MALFORMATION;

EID: 69049094907     PISSN: 10792104     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tripleo.2009.04.035     Document Type: Article
Times cited : (12)

References (12)
  • 1
    • 0016809496 scopus 로고
    • The KBG syndrome: a syndrome of short stature, characteristic facies, mental retardation, macrodontia and skeletal anomalies
    • Herrmann J., Pallister P.D., Tiddy W., and Opitz J.M. The KBG syndrome: a syndrome of short stature, characteristic facies, mental retardation, macrodontia and skeletal anomalies. Birth Defects Orig Artic Ser 11 (1975) 7-18
    • (1975) Birth Defects Orig Artic Ser , vol.11 , pp. 7-18
    • Herrmann, J.1    Pallister, P.D.2    Tiddy, W.3    Opitz, J.M.4
  • 2
    • 4744348389 scopus 로고    scopus 로고
    • The KBG syndrome: confirmation of autosomal dominant inheritance and further delineation of the phenotype
    • Tekin M., Kavaz A., Berberoglu M., Fitoz S., Ekim M., Ocal G., et al. The KBG syndrome: confirmation of autosomal dominant inheritance and further delineation of the phenotype. Am J Med Genet Part A 130A (2004) 284-287
    • (2004) Am J Med Genet Part A , vol.130 A , pp. 284-287
    • Tekin, M.1    Kavaz, A.2    Berberoglu, M.3    Fitoz, S.4    Ekim, M.5    Ocal, G.6
  • 6
    • 33846849462 scopus 로고    scopus 로고
    • KBG syndrome: report of twins, neurological characteristics, and delineation of diagnostic criteria
    • Skjei K.L., Martin M.M., and Slavotinek A.M. KBG syndrome: report of twins, neurological characteristics, and delineation of diagnostic criteria. Am J Med Genet Part A 143A (2007) 292-300
    • (2007) Am J Med Genet Part A , vol.143 A , pp. 292-300
    • Skjei, K.L.1    Martin, M.M.2    Slavotinek, A.M.3
  • 7
    • 0028102429 scopus 로고
    • Six additional cases of the KBG syndrome: clinical reports and outline of the diagnostic criteria
    • Zollino M., Battaglia A., D'Avanzo M.G., Della Bruna M.M., Marini R., Scarano G., et al. Six additional cases of the KBG syndrome: clinical reports and outline of the diagnostic criteria. Am J Med Genet 52 (1994) 302-307
    • (1994) Am J Med Genet , vol.52 , pp. 302-307
    • Zollino, M.1    Battaglia, A.2    D'Avanzo, M.G.3    Della Bruna, M.M.4    Marini, R.5    Scarano, G.6
  • 9
    • 0031755792 scopus 로고    scopus 로고
    • Further delineation of the KBG syndrome
    • Devriendt K., Holvoet M., and Fryns J.P. Further delineation of the KBG syndrome. Genet Couns 9 (1998) 191-194
    • (1998) Genet Couns , vol.9 , pp. 191-194
    • Devriendt, K.1    Holvoet, M.2    Fryns, J.P.3
  • 11
    • 0017748579 scopus 로고
    • Short stature, craniofacial dysmorphism and dento-skeletal abnormalities in a large kindred. A variant of K.B.G. syndrome or a new mental retardation syndrome
    • Parloir C., Fryns J.P., Deroover J., Lebas E., Goffaux P., and van den Berghe H. Short stature, craniofacial dysmorphism and dento-skeletal abnormalities in a large kindred. A variant of K.B.G. syndrome or a new mental retardation syndrome. Clin Genet 12 (1977) 263-266
    • (1977) Clin Genet , vol.12 , pp. 263-266
    • Parloir, C.1    Fryns, J.P.2    Deroover, J.3    Lebas, E.4    Goffaux, P.5    van den Berghe, H.6
  • 12
    • 42149122010 scopus 로고    scopus 로고
    • Taurodontism: a review of the condition and endodontic treatment challenges
    • Jafarzadeh H., Azarpazhooh A., and Mayhall J.T. Taurodontism: a review of the condition and endodontic treatment challenges. Int Endodontic J 41 (2008) 375-388
    • (2008) Int Endodontic J , vol.41 , pp. 375-388
    • Jafarzadeh, H.1    Azarpazhooh, A.2    Mayhall, J.T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.