-
1
-
-
0016809496
-
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
-
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
-
4
-
-
9644278315
-
KBG syndrome in a cohort of Italian patients
-
Brancati F., D'Avanzo M.G., Digilio M.C., Sarkozy A., Biondi M., De Brasi D., et al. KBG syndrome in a cohort of Italian patients. Am J Med Genet Part A 131A (2004) 144-149
-
(2004)
Am J Med Genet Part A
, vol.131 A
, pp. 144-149
-
-
Brancati, F.1
D'Avanzo, M.G.2
Digilio, M.C.3
Sarkozy, A.4
Biondi, M.5
De Brasi, D.6
-
5
-
-
9644303422
-
Clinical variability in KBG syndrome: report of three unrelated families
-
Maegawa G.H., Leite J.C., Felix T.M., Da Silveira H.L., and Da Silveira H.E. Clinical variability in KBG syndrome: report of three unrelated families. Am J Med Genet A 131 (2004) 150-154
-
(2004)
Am J Med Genet A
, vol.131
, pp. 150-154
-
-
Maegawa, G.H.1
Leite, J.C.2
Felix, T.M.3
Da Silveira, H.L.4
Da Silveira, H.E.5
-
6
-
-
33846849462
-
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
-
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
-
10
-
-
0035292724
-
The KBG syndrome, characteristic dental findings: a case report
-
Dowling P.A., Fleming P., Gorlin R.J., King M., Nevin N.C., and McEntagart M. The KBG syndrome, characteristic dental findings: a case report. Int J Paediatr Dent 11 (2001) 131-134
-
(2001)
Int J Paediatr Dent
, vol.11
, pp. 131-134
-
-
Dowling, P.A.1
Fleming, P.2
Gorlin, R.J.3
King, M.4
Nevin, N.C.5
McEntagart, M.6
-
11
-
-
0017748579
-
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
-
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
|